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CTNNB1 p.Glu692=

c.2076G>A · VCV4712370

Uncertain significance Single submitter
Classification
Uncertain significance
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Absent
absent from gnomAD v4.1

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation/SpliceAI carries the signal.
Splicing
SpliceAIΔ0.76donor gain · deltas
PangolinΔ0.83loss · gain 0.63 · SpliceAI calls gain · independent
Constraint at this position
ConservationphyloP 9.9GERP 1.9, phastCons 1
Overall
CADD23.5PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Absent from gnomAD v4.1. Not observed in any sequenced alleles — a rarity signal (ACMG PM2-supporting), not evidence of pathogenicity on its own.

Variant & gene context

Gene
CTNNB1
Protein
p.Glu692=
Coding
c.2076G>A
MANE Select
NM_001904
Type
single nucleotide variant
Location
chr3:41236709 (GRCh38)
Gene constraint
LOEUF 0.139 · pLI 1.00 · ClinGen HI 3/3 (gnomAD)
Structure
AlphaFold pLDDT 81.02 · 50 PDB
Residue 692
a UniProt-annotated variant site (in nedsdv; the patient also manifest features of exudative vitreoretinopathy)
Full CTNNB1 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Similar variants

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/ctnnb1-p-glu692 (accessed [today's date]).

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