Is DVL1 p.Arg149Gln (c.446G>A) pathogenic?

DVL1 p.Arg149Gln (c.446G>A) is classified Uncertain significance in DVL1 (ClinVar, Multiple submitters, 2 submitters; last evaluated 2025-06-19). AlphaMissense: likely benign (0.115); Very rare (popmax 0.00841%, nfe); Associated with Inborn genetic diseases.

What condition is associated with DVL1 p.Arg149Gln (c.446G>A)?

DVL1 p.Arg149Gln (c.446G>A) is associated with Inborn genetic diseases (ClinVar).

How common is DVL1 p.Arg149Gln (c.446G>A) in the general population?

DVL1 p.Arg149Gln (c.446G>A) is very rare (popmax 0.00841%, nfe) (gnomAD).

What do computational predictors say about DVL1 p.Arg149Gln (c.446G>A)?

AlphaMissense predicts likely benign (score 0.115) — an in-silico prediction, not a clinical call.

DVL1 p.Arg149Gln

c.446G>A · rs998424030 · VCV3086380

Uncertain significance Multiple submitters

Classification

Uncertain significance

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 2 submitters

AlphaMissense

likely benign

0.115 · ACMG-weighted

gnomAD v4.1

Rare

very rare (popmax 0.00841%, nfe)

Missense predictors

0/3 damaging

AlphaMissense, REVEL, SaProt

Conditions

Inborn genetic diseases

Computational evidence

Protein change
AlphaMissense	0.115	likely benign
REVEL	0.145	moderately benign-leaning
SaProt	LLR -8.99	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 5.9	GERP 2.5, phastCons 1
Regional constraint	o/e 1.15	unconstrained · MANE · 13 kb · p 2.8e-06 · regional, not allelic
Overall
CADD	29.1	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 0.00841% European (non-Finnish) · 98/1,165,600 alleles

Filtering AF 0.00706% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.00649%

Overall 0.00644% 102/1,584,046 alleles · very rare

Ancestry group	Frequency	1 in
European (non-Finnish)grpmax	0.00841%	11,894
East Asian	0.0046%	21,745
Remaining individualsnot grpmax-eligible	0.00327%	30,625

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: DVL1
Protein: p.Arg149Gln
Coding: c.446G>A
MANE Select: NM_001330311
dbSNP: rs998424030
Type: single nucleotide variant
Location: chr1:1342073 (GRCh38)
Gene constraint: LOEUF 1.046 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 60.70 · 3 PDB
Residue 149: the 'disordered' region

Full DVL1 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

DVL1 p.Arg149Gly Uncertain significance ★ ⚠ same residue
DVL1 p.Ala125Val Uncertain significance ★★ ⚠ same condition
DVL1 p.Ala288Val Uncertain significance ★★ ⚠ same condition
DVL1 p.Ala361Thr Uncertain significance ★★ ⚠ same condition
DVL1 p.Ala368Val Uncertain significance ★★ ⚠ same condition
DVL1 p.Ala667Pro Uncertain significance ★★ ⚠ same condition
DVL1 p.Arg108Trp Uncertain significance ★★ ⚠ same condition
DVL1 p.Arg150Cys 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/dvl1-p-arg149gln (accessed [today's date]).

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