Is INTS1 p.Arg1841His (c.5522G>A) pathogenic?

INTS1 p.Arg1841His (c.5522G>A) is classified Uncertain significance in INTS1 (ClinVar, Single submitter, 1 submitter; last evaluated 2022-11-30). AlphaMissense: likely benign (0.2368); Very rare (popmax 0.00342%, nfe); Associated with Inborn genetic diseases.

What condition is associated with INTS1 p.Arg1841His (c.5522G>A)?

INTS1 p.Arg1841His (c.5522G>A) is associated with Inborn genetic diseases (ClinVar).

How common is INTS1 p.Arg1841His (c.5522G>A) in the general population?

INTS1 p.Arg1841His (c.5522G>A) is very rare (popmax 0.00342%, nfe) (gnomAD).

What do computational predictors say about INTS1 p.Arg1841His (c.5522G>A)?

AlphaMissense predicts likely benign (score 0.2368) — an in-silico prediction, not a clinical call.

INTS1 p.Arg1841His

c.5522G>A · rs780284734 · VCV2329592

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

likely benign

0.2368 · ACMG-weighted

gnomAD v4.1

Rare

very rare (popmax 0.00342%, nfe)

Missense predictors

0/2 damaging

AlphaMissense, SaProt · REVEL no call

Conditions

Inborn genetic diseases

Computational evidence

Protein change
AlphaMissense	0.2368	likely benign
REVEL	0.292	indeterminate
SaProt	LLR -5.79	tolerated
⇒ AlphaMissense and SaProt both call this tolerated; REVEL makes no call.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 5.9	GERP 0.1, phastCons 1
Regional constraint	o/e 1.09	unconstrained · MANE · 12 kb · p 0.001 · regional, not allelic
Overall
CADD	24.9	PHRED · no single calibrated threshold — expert panels disagree

ClinVar classifies this uncertain; the computational predictors unanimously lean tolerated — 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

Grpmax group 0.00342% European (non-Finnish) · 40/1,170,936 alleles

Filtering AF 0.00258% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.00227%

Overall 0.00277% 44/1,590,190 alleles · very rare exomes 41/1,437,982 · genomes 3/152,208 · joint denominator

Ancestry group	Frequency	1 in
European (non-Finnish)grpmax	0.00342%	29,273
African / African-American	0.00269%	37,236
Remaining individualsnot grpmax-eligible	0.00163%	61,496
South Asian	0.00115%	87,050

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: INTS1
Protein: p.Arg1841His
Coding: c.5522G>A
MANE Select: NM_001080453
dbSNP: rs780284734
Type: single nucleotide variant
Location: chr7:1474819 (GRCh38)
Gene constraint: LOEUF 0.785 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 75.49 · 8 PDB
Residue 1841: an α-helix; a UniProt-annotated variant site (in ndcagf; decreased protein abundance)

Full INTS1 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

Inborn genetic diseases — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Similar variants

INTS1 p.Arg1841Cys Uncertain significance ★★ ⚠ same residue
INTS1 c.1283+5G>A Uncertain significance ★★ same condition
INTS1 c.2977-5C>T Uncertain significance ★★ same condition
INTS1 p.Ala1505Val Uncertain significance ★★ ⚠ same condition
INTS1 p.Ala1854Val Uncertain significance ★★ ⚠ same condition
INTS1 p.Ala2155Val Uncertain significance ★★ ⚠ same condition
INTS1 p.Ala2175Thr Uncertain significance ★★ ⚠ same condition
INTS1 p.Ala4Thr 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/ints1-p-arg1841his (accessed [today's date]).

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