Is STAT1 p.Thr342Pro (c.1024A>C) pathogenic?

STAT1 p.Thr342Pro (c.1024A>C) is classified Uncertain significance in STAT1 (ClinVar, Single submitter, 1 submitter; last evaluated 2016-11-01). AlphaMissense: likely pathogenic (0.9492); Absent from gnomAD v4.1.

How common is STAT1 p.Thr342Pro (c.1024A>C) in the general population?

STAT1 p.Thr342Pro (c.1024A>C) is absent from gnomAD v4.1 (gnomAD).

What do computational predictors say about STAT1 p.Thr342Pro (c.1024A>C)?

AlphaMissense predicts likely pathogenic (score 0.9492) — an in-silico prediction, not a clinical call.

STAT1 p.Thr342Pro

c.1024A>C · rs1064797279 · VCV425253

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

likely pathogenic

0.9492 · ACMG-weighted

gnomAD v4.1

Absent

absent from gnomAD v4.1

Missense predictors

3/3 damaging

AlphaMissense, REVEL, SaProt

Computational evidence

Protein change
AlphaMissense	0.9492	likely pathogenic
REVEL	0.945	strongly pathogenic-leaning
SaProt	LLR -15.41	damaging
⇒ AlphaMissense, REVEL and SaProt all call this damaging.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 7.8	GERP 1.9, phastCons 1
Regional constraint	o/e 0.19	constrained · MANE · 9,439 bp · p 1.9e-19 · regional, not allelic
Overall
CADD	29.4	PHRED · no single calibrated threshold — expert panels disagree

ClinVar classifies this uncertain; the computational predictors unanimously lean damaging — 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: STAT1
Protein: p.Thr342Pro
Coding: c.1024A>C
MANE Select: NM_007315
dbSNP: rs1064797279
Type: single nucleotide variant
Location: chr2:190991241 (GRCh38)
Gene constraint: LOEUF 0.271 · pLI 1.00 · ClinGen HI 0/3 (gnomAD)
Structure: AlphaFold pLDDT 87.78 · 10 PDB
Residue 342: a β-strand

Full STAT1 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Similar variants

STAT1 p.Ala267Val Pathogenic ★★ ⚠ same type
STAT1 p.Arg274Gln Pathogenic ★★ ⚠ same type
STAT1 p.Arg274Gly Pathogenic/Likely pathogenic ★★ same type
STAT1 p.Arg274Trp Pathogenic ★★ same type
STAT1 p.Asp171Asn Likely pathogenic ★★ ⚠ same type
STAT1 p.Asp292Glu Likely pathogenic ★★ ⚠ same type
STAT1 p.Cys324Arg Likely pathogenic ★★ same type
STAT1 p.Gln271Pro Pathogenic/Likely pathogenic ★★ ⚠ 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/stat1-p-thr342pro (accessed [today's date]).

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