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AIRE p.Glu354fs

c.1062del · VCV4818284

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 polyendocrine syndrome type 1

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Consequenceframeshiftpredicted loss-of-function
NMDpredictedpremature termination codon in exon 9 of 14
Splicing
SpliceAI—not assessed · substitutions only
Constraint at this position
ConservationphyloP 1.1GERP -0.42, phastCons 0.001

Predicted loss-of-function is descriptive, not an applied PVS1 code.

Variant & gene context

Gene
AIRE
Protein
p.Glu354fs
Coding
c.1062del
MANE Select
NM_000383
Type
Deletion
Location
chr21:44292368 (GRCh38)
Gene constraint
LOEUF 1.169 · pLI <0.01 (gnomAD)
Structure
AlphaFold pLDDT 62.30 · 4 PDB
Residue 354
the 'disordered' region
Full AIRE gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

autoimmune polyendocrine syndrome type 1 — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

For Autoimmune polyendocrinopathy type 1 (Orphanet):

Inheritance
Autosomal recessive
Onset
Adolescent, Childhood
Prevalence
1-9 / 100 000 (Finland)

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/aire-p-glu354fs (accessed [today's date]).

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