Is CUX2 p.Pro834Ala (c.2500C>G) pathogenic?

CUX2 p.Pro834Ala (c.2500C>G) is classified Benign/Likely benign in CUX2 (ClinVar, Multiple submitters, 4 submitters; last evaluated 2025-08-10). AlphaMissense: likely benign (0.0486); Rare (popmax 0.153%, nfe); Associated with Inborn genetic diseases.

What condition is associated with CUX2 p.Pro834Ala (c.2500C>G)?

CUX2 p.Pro834Ala (c.2500C>G) is associated with Inborn genetic diseases (ClinVar).

How common is CUX2 p.Pro834Ala (c.2500C>G) in the general population?

CUX2 p.Pro834Ala (c.2500C>G) is rare (popmax 0.153%, nfe) (gnomAD).

What do computational predictors say about CUX2 p.Pro834Ala (c.2500C>G)?

AlphaMissense predicts likely benign (score 0.0486) — an in-silico prediction, not a clinical call.

CUX2 p.Pro834Ala

c.2500C>G · rs750555630 · VCV2570847

Benign/Likely benign Multiple submitters

Classification

Benign/Likely benign

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 4 submitters

AlphaMissense

likely benign

0.0486 · ACMG-weighted

gnomAD v4.1

Rare

rare (popmax 0.153%, nfe)

Missense predictors

0/3 damaging

AlphaMissense, REVEL, SaProt

Conditions

Inborn genetic diseases

Computational evidence

Protein change
AlphaMissense	0.0486	likely benign
REVEL	0.048	moderately benign-leaning
SaProt	LLR -5.72	tolerated
⇒ AlphaMissense, REVEL and SaProt all call this tolerated.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 0.36	GERP -2.7, phastCons 0.004
Regional constraint	o/e 1.01	unconstrained · MANE · 8,582 bp · p 0.88 · regional, not allelic
Overall
CADD	0.593	PHRED · no single calibrated threshold — expert panels disagree

AlphaMissense carries the ACMG weight for missense; REVEL and SaProt are independent agreement signals.

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.153% European (non-Finnish) · 1,782/1,168,370 alleles

Filtering AF 0.147% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.144%

Overall 0.128% 2,026/1,578,528 alleles · rare

Ancestry group	Frequency	1 in
Finnishnot grpmax-eligible	0.261%	383
European (non-Finnish)grpmax	0.153%	656
Remaining individualsnot grpmax-eligible	0.14%	714
Middle Eastern	0.0167%	5,998
South Asian	0.0157%	6,372
Admixed American	0.0138%	7,253
African / African-American	0.0122%	8,169

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: CUX2
Protein: p.Pro834Ala
Coding: c.2500C>G
MANE Select: NM_015267
dbSNP: rs750555630
Type: single nucleotide variant
Location: chr12:111320509 (GRCh38)
Gene constraint: LOEUF 0.383 · pLI 1.00 (gnomAD)
Structure: AlphaFold pLDDT 60.99 · 3 PDB
Residue 834: the 'disordered' region

Full CUX2 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

Inborn genetic diseases — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Similar variants

CUX2 p.Pro834Arg Uncertain significance ★★ ⚠ same residue
CUX2 p.Ala302Ser Uncertain significance ★★ ⚠ same condition
CUX2 p.Ala336Thr Uncertain significance ★★ ⚠ same condition
CUX2 p.Arg312Gln Uncertain significance ★★ ⚠ same condition
CUX2 p.Arg701His Uncertain significance ★★ ⚠ same condition
CUX2 p.Arg954Cys Uncertain significance ★★ ⚠ same condition
CUX2 p.Asp1334Asn Uncertain significance ★★ ⚠ same condition
CUX2 p.Asp844Gly 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/cux2-p-pro834ala (accessed [today's date]).

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