Is ARX p.Thr368= (c.1104C>T) pathogenic?

ARX p.Thr368= (c.1104C>T) is classified Likely benign in ARX (ClinVar, Single submitter, 1 submitter; last evaluated 2023-11-06). Ultra-rare (popmax 0.0231%, mid); Associated with intellectual disability, X-linked, with or without seizures, ARX-related.

How common is ARX p.Thr368= (c.1104C>T) in the general population?

ARX p.Thr368= (c.1104C>T) is ultra-rare (popmax 0.0231%, mid) (gnomAD).

ARX p.Thr368=

Q: What condition is associated with ARX p.Thr368= (c.1104C>T)?

ARX p.Thr368= (c.1104C>T) is associated with intellectual disability, X-linked, with or without seizures, ARX-related, developmental and epileptic encephalopathy, 1 (ClinVar).

c.1104C>T · rs771822246 · VCV759318

Likely benign Single submitter

Classification

Likely benign

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

gnomAD v4.1

Rare

ultra-rare (popmax 0.0231%, mid)

Conditions

intellectual disability, X-linked, with or without seizures, ARX-related

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 -0.12	GERP -4.3, phastCons 0.009
Overall
CADD	3.176	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.0231% Middle Eastern · 1/4,334 alleles

Filtering AF 0.000607% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.000227%

Overall 0.000835% 10/1,198,151 alleles · ultra-rare

Ancestry group	Frequency	1 in
Middle Easterngrpmax	0.0231%	4,334
Finnishnot grpmax-eligible	0.00442%	22,643
African / African-American	0.00366%	27,343
East Asian	0.00302%	33,157
Admixed American	0.00224%	44,669
South Asian	0.00178%	56,145
European (non-Finnish)	0.000225%	445,145

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: ARX
Protein: p.Thr368=
Coding: c.1104C>T
MANE Select: NM_139058
dbSNP: rs771822246
Type: single nucleotide variant
Location: chrX:25010275 (GRCh38)
Structure: AlphaFold pLDDT 56.51
Residue 368: a DNA-binding region

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

Disease context

intellectual disability, X-linked, with or without seizures, ARX-related — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Also linked: developmental and epileptic encephalopathy, 1

Similar variants

ARX p.Arg330His Likely pathogenic ★★ same condition
ARX p.Arg332Gly Pathogenic/Likely pathogenic ★★ same condition
ARX p.Arg332His Pathogenic ★★ same condition
ARX p.Arg371Gln Likely pathogenic ★★ same condition
ARX p.Arg371Ter Pathogenic ★★ same condition
ARX p.Arg384Cys Pathogenic/Likely pathogenic ★★ same condition
ARX p.Glu294Ter Pathogenic ★★ same condition
ARX p.Pro353Leu 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/arx-p-thr368 (accessed [today's date]).

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