Is CEBPG p.Ala37Val (c.110C>T) pathogenic?

CEBPG p.Ala37Val (c.110C>T) is classified Uncertain significance in CEBPG (ClinVar, Single submitter, 1 submitter; last evaluated 2023-04-04). AlphaMissense: likely benign (0.0805); Absent from gnomAD v4.1.

How common is CEBPG p.Ala37Val (c.110C>T) in the general population?

CEBPG p.Ala37Val (c.110C>T) is absent from gnomAD v4.1 (gnomAD).

What do computational predictors say about CEBPG p.Ala37Val (c.110C>T)?

AlphaMissense predicts likely benign (score 0.0805) — an in-silico prediction, not a clinical call.

CEBPG p.Ala37Val

c.110C>T · rs778709948 · VCV2532832

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

likely benign

0.0805 · ACMG-weighted

gnomAD v4.1

Absent

absent from gnomAD v4.1

Missense predictors

0/3 damaging

AlphaMissense, REVEL, SaProt

Computational evidence

Protein change
AlphaMissense	0.0805	likely benign
REVEL	0.079	moderately benign-leaning
SaProt	LLR -6.01	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 4.8	GERP 2.1, phastCons 1
Regional constraint	o/e 0.86	unconstrained · MANE · 449 bp · p 0.054 · regional, not allelic
Overall
CADD	21.5	PHRED · no single calibrated threshold — expert panels disagree

ClinVar classifies this uncertain; the computational predictors unanimously lean tolerated — a triage signal, not a reclassification

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

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: CEBPG
Protein: p.Ala37Val
Coding: c.110C>T
MANE Select: NM_001806
dbSNP: rs778709948
Type: single nucleotide variant
Location: chr19:33379349 (GRCh38)
Gene constraint: LOEUF 1.072 · pLI 0.04 (gnomAD)
Structure: AlphaFold pLDDT 76.64
Residue 37: the 'disordered' region

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

Similar variants

CEBPG p.Ala37Ser Uncertain significance ★ ⚠ same residue
CEBPG p.Arg68Cys Uncertain significance ★ ⚠ same type
CEBPG p.Asp131Asn Uncertain significance ★ ⚠ same type
CEBPG p.Gln88Lys Uncertain significance ★ ⚠ same type
CEBPG p.Gly145Asp Uncertain significance ★ ⚠ same type
CEBPG p.Gly15Arg Uncertain significance ★ ⚠ same type
CEBPG p.Gly40Ala Uncertain significance ★ ⚠ same type
CEBPG p.Gly40Arg 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/cebpg-p-ala37val (accessed [today's date]).

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