Is ARRDC1 p.Val208Met (c.622G>A) pathogenic?

ARRDC1 p.Val208Met (c.622G>A) is classified Uncertain significance in ARRDC1 (ClinVar, Single submitter, 1 submitter; last evaluated 2024-09-09). AlphaMissense: likely pathogenic (0.6922); Very rare (popmax 0.00171%, nfe).

How common is ARRDC1 p.Val208Met (c.622G>A) in the general population?

ARRDC1 p.Val208Met (c.622G>A) is very rare (popmax 0.00171%, nfe) (gnomAD).

What do computational predictors say about ARRDC1 p.Val208Met (c.622G>A)?

AlphaMissense predicts likely pathogenic (score 0.6922) — an in-silico prediction, not a clinical call.

ARRDC1 p.Val208Met

c.622G>A · VCV3431931

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

likely pathogenic

0.6922 · ACMG-weighted

gnomAD v4.1

Rare

very rare (popmax 0.00171%, nfe)

Missense predictors

2/3 damaging

AlphaMissense, REVEL, SaProt

Computational evidence

Protein change
AlphaMissense	0.6922	likely pathogenic
REVEL	0.288	benign-leaning
SaProt	LLR -10.71	damaging
⇒ AlphaMissense and SaProt call this damaging; REVEL does not.
Splicing
SpliceAI	Δ0.88	acceptor loss, 1 bp away · masked 0 · deltas
Constraint at this position
Conservation	phyloP 9.8	GERP 6, phastCons 1
Regional constraint	o/e 1.10	unconstrained · MANE · 9,417 bp · p 0.014 · regional, not allelic
Overall
CADD	29.2	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

Grpmax group 0.00171% European (non-Finnish) · 20/1,166,798 alleles

Filtering AF 0.00112% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.00091%

Overall 0.00126% 20/1,591,276 alleles · very rare

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: ARRDC1
Protein: p.Val208Met
Coding: c.622G>A
MANE Select: NM_152285
Type: single nucleotide variant
Location: chr9:137614302 (GRCh38)
Gene constraint: LOEUF 1.191 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 78.34

Full ARRDC1 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Similar variants

ARRDC1 p.Ala223Val Uncertain significance ★ ⚠ same type
ARRDC1 p.Ala228Val Uncertain significance ★ ⚠ same type
ARRDC1 p.Ala25Ser Uncertain significance ★ ⚠ same type
ARRDC1 p.Ala285Thr Uncertain significance ★ ⚠ same type
ARRDC1 p.Ala311Thr Uncertain significance ★ ⚠ same type
ARRDC1 p.Ala34Val Uncertain significance ★ ⚠ same type
ARRDC1 p.Ala94Val Uncertain significance ★ ⚠ same type
ARRDC1 p.Arg119Gln 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/arrdc1-p-val208met (accessed [today's date]).

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