STAT1 p.Lys361fs
c.1082_1083del · VCV3775677
Likely pathogenic
Single submitter
Classification
Likely pathogenic
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
Consequence
frameshift
predicted LoF
gnomAD v4.1
Rare
Conditions
1
autoimmune enteropathy and endocrinopathy - susceptibility to chronic infections syndrome
Computational evidence
| Protein change | ||
| Missense predictors do not apply to this variant type; conservation carries the signal. | ||
| Consequence | frameshift | predicted loss-of-function in a LoF-intolerant gene |
|---|---|---|
| NMD | predicted | premature termination codon in exon 12 of 25 |
| Splicing | ||
| SpliceAI | — | not assessed · substitutions only |
| Constraint at this position | ||
| Conservation | phyloP 7.6 | GERP 1.7, phastCons 1 |
Predicted loss-of-function is descriptive, not an applied PVS1 code.
Variant & gene context
- Gene
- STAT1
- Protein
- p.Lys361fs
- Coding
- c.1082_1083del
- MANE Select
- NM_007315
- Type
- Deletion
- Location
- chr2:190989629 (GRCh38)
- Gene constraint
- LOEUF 0.271 · pLI 1.00 · ClinGen HI 0/3 (gnomAD)
- Structure
- AlphaFold pLDDT 87.78 · 10 PDB
- Residue 361
- a β-strand
Disease context
autoimmune enteropathy and endocrinopathy - susceptibility to chronic infections syndrome — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatmentsFor STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome (Orphanet):
- Inheritance
- Autosomal dominant
- Onset
- Infancy
Similar variants
- STAT1 p.Val339fs Pathogenic ★★ same condition
- STAT1 p.Asp257fs Pathogenic ★ same condition
- STAT1 p.Glu411fs Pathogenic ★ same condition
- STAT1 p.Ile232fs Pathogenic ★ same condition
- STAT1 p.Ile612fs Pathogenic ★ same condition
- STAT1 p.Leu667fs Pathogenic ★ same condition
- STAT1 c.1632+6del Uncertain significance ★ same condition
- STAT1 c.2059+6_2059+7del 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/stat1-p-lys361fs (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown