Is FAAH p.Gln577Arg (c.1730A>G) pathogenic?

FAAH p.Gln577Arg (c.1730A>G) is classified Likely benign in FAAH (ClinVar, Single submitter, 1 submitter; last evaluated 2025-02-19). AlphaMissense: likely benign (0.0567); Absent from gnomAD v4.1.

How common is FAAH p.Gln577Arg (c.1730A>G) in the general population?

FAAH p.Gln577Arg (c.1730A>G) is absent from gnomAD v4.1 (gnomAD).

What do computational predictors say about FAAH p.Gln577Arg (c.1730A>G)?

AlphaMissense predicts likely benign (score 0.0567) — an in-silico prediction, not a clinical call.

FAAH p.Gln577Arg

c.1730A>G · VCV3847058

Likely benign Single submitter

Classification

Likely benign

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

likely benign

0.0567 · ACMG-weighted

gnomAD v4.1

Absent

absent from gnomAD v4.1

Missense predictors

0/3 damaging

AlphaMissense, REVEL, SaProt

Computational evidence

Protein change
AlphaMissense	0.0567	likely benign
REVEL	0.037	moderately benign-leaning
SaProt	LLR -5.90	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 -0.68	GERP -4.1, phastCons 0.83
Regional constraint	o/e 0.90	unconstrained · MANE · 19 kb · p 0.0063 · regional, not allelic
Overall
CADD	0.003	PHRED · no single calibrated threshold — expert panels disagree

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: FAAH
Protein: p.Gln577Arg
Coding: c.1730A>G
MANE Select: NM_001441
Type: single nucleotide variant
Location: chr1:46413565 (GRCh38)
Gene constraint: LOEUF 1.147 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 95.44

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

Similar variants

FAAH c.1316+3A>G Benign ★★ same type
FAAH p.Ala356Val Benign ★★ same type
FAAH p.Ala476Gly Benign ★★ same type
FAAH p.Arg439= Benign ★★ same type
FAAH p.Gly544= Benign ★★ same type
FAAH p.Leu426= Benign ★★ same type
FAAH p.Lys263= Benign ★★ same type
FAAH p.Pro129Thr Benign/Likely benign ★★ ⚠ 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/faah-p-gln577arg (accessed [today's date]).

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