Is SATB2 p.Thr151= (c.453G>A) pathogenic?

SATB2 p.Thr151= (c.453G>A) is classified Likely benign in SATB2 (ClinVar, Multiple submitters, 2 submitters; last evaluated 2025-02-24). Ultra-rare (popmax 0.0164%, mid); Associated with chromosome 2q32-q33 deletion syndrome.

What condition is associated with SATB2 p.Thr151= (c.453G>A)?

SATB2 p.Thr151= (c.453G>A) is associated with chromosome 2q32-q33 deletion syndrome (ClinVar).

How common is SATB2 p.Thr151= (c.453G>A) in the general population?

SATB2 p.Thr151= (c.453G>A) is ultra-rare (popmax 0.0164%, mid) (gnomAD).

SATB2 p.Thr151=

c.453G>A · rs973674250 · VCV469560

Likely benign Multiple submitters

Classification

Likely benign

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 2 submitters

gnomAD v4.1

Rare

ultra-rare (popmax 0.0164%, mid)

Conditions

chromosome 2q32-q33 deletion syndrome

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 -2.6	GERP -0.24
Overall
CADD	9.85	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.0164% Middle Eastern · 1/6,084 alleles

Filtering AF 0.00347% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.00229%

Overall 0.00136% 22/1,613,998 alleles · ultra-rare exomes 17/1,461,800 · genomes 5/152,198 · joint denominator

Ancestry group	Frequency	1 in
Middle Easterngrpmax	0.0164%	6,084
African / African-American	0.00801%	12,486
Remaining individualsnot grpmax-eligible	0.0048%	20,827
East Asian	0.00223%	44,896
European (non-Finnish)	0.000932%	107,271

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: SATB2
Protein: p.Thr151=
Coding: c.453G>A
MANE Select: NM_001172509
dbSNP: rs973674250
Type: single nucleotide variant
Location: chr2:199381714 (GRCh38)
Gene constraint: LOEUF 0.077 · pLI 1.00 · ClinGen HI 3/3 (gnomAD)
Structure: AlphaFold pLDDT 66.87 · 3 PDB
Residue 151: the cmp domain

Full SATB2 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

chromosome 2q32-q33 deletion syndrome — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Similar variants

SATB2 p.Thr151Met Uncertain significance ★★ ⚠ same residue
SATB2 c.1174-2A>G Pathogenic ★★ same condition
SATB2 c.474-2A>G Pathogenic ★★ same condition
SATB2 c.597+1G>A Pathogenic/Likely pathogenic ★★ same condition
SATB2 c.700+1G>A Likely pathogenic ★★ same condition
SATB2 p.Arg239Ter Pathogenic ★★ same condition
SATB2 p.Arg283Ter Pathogenic ★★ same condition
SATB2 p.Arg389Cys Pathogenic/Likely pathogenic ★★ 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/satb2-p-thr151 (accessed [today's date]).

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