Is ECT2 p.His912Arg (c.2735A>G) pathogenic?

ECT2 p.His912Arg (c.2735A>G) is classified Uncertain significance in ECT2 (ClinVar, Multiple submitters, 2 submitters; last evaluated 2021-07-09). AlphaMissense: likely benign (0.2273); Ultra-rare (popmax 0.0331%, mid).

How common is ECT2 p.His912Arg (c.2735A>G) in the general population?

ECT2 p.His912Arg (c.2735A>G) is ultra-rare (popmax 0.0331%, mid) (gnomAD).

What do computational predictors say about ECT2 p.His912Arg (c.2735A>G)?

AlphaMissense predicts likely benign (score 0.2273) — an in-silico prediction, not a clinical call.

ECT2 p.His912Arg

c.2735A>G · rs766107326 · VCV2235669

Uncertain significance Multiple submitters

Classification

Uncertain significance

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 2 submitters

AlphaMissense

likely benign

0.2273 · ACMG-weighted

gnomAD v4.1

Rare

ultra-rare (popmax 0.0331%, mid)

Missense predictors

0/3 damaging

AlphaMissense, REVEL, SaProt

Computational evidence

Protein change
AlphaMissense	0.2273	likely benign
REVEL	0.159	moderately benign-leaning
SaProt	LLR -6.16	tolerated
⇒ AlphaMissense, REVEL and SaProt all call this tolerated.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 11	GERP 1.7, phastCons 1
Regional constraint	o/e 0.87	unconstrained · MANE · 66 kb · p 1.6e-05 · regional, not allelic
Overall
CADD	24.1	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 0.0331% Middle Eastern · 2/6,036 alleles

Filtering AF 0.00584% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.00243%

Overall 0.000624% 10/1,603,418 alleles · ultra-rare exomes 9/1,451,340 · genomes 1/152,078 · joint denominator

Ancestry group	Frequency	1 in
Middle Easterngrpmax	0.0331%	3,018
Remaining individualsnot grpmax-eligible	0.00161%	62,016
European (non-Finnish)	0.000596%	167,729

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: ECT2
Protein: p.His912Arg
Coding: c.2735A>G
MANE Select: NM_001258315
dbSNP: rs766107326
Type: single nucleotide variant
Location: chr3:172820227 (GRCh38)
Gene constraint: LOEUF 0.664 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 71.17 · 3 PDB

Full ECT2 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Similar variants

ECT2 p.Pro236Ala Uncertain significance ★★ ⚠ same type
ECT2 p.Pro481= Benign ★★ same type
ECT2 c.1069-2A>G Uncertain significance ★ same type
ECT2 p.Ala258Thr Uncertain significance ★ ⚠ same type
ECT2 p.Ala850Thr Uncertain significance ★ ⚠ same type
ECT2 p.Arg169Cys Uncertain significance ★ ⚠ same type
ECT2 p.Arg194Met Uncertain significance ★ ⚠ same type
ECT2 p.Arg228Lys Uncertain significance ★ ⚠ 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/ect2-p-his912arg (accessed [today's date]).

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