Is DVL1 p.Arg233= (c.699G>T) pathogenic?

DVL1 p.Arg233= (c.699G>T) is classified Uncertain significance in DVL1 (ClinVar, Single submitter, 1 submitter; last evaluated 2022-08-12). Very rare (popmax 0.00882%, nfe).

How common is DVL1 p.Arg233= (c.699G>T) in the general population?

DVL1 p.Arg233= (c.699G>T) is very rare (popmax 0.00882%, nfe) (gnomAD).

DVL1 p.Arg233=

c.699G>T · rs771135299 · VCV843496

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

gnomAD v4.1

Rare

very rare (popmax 0.00882%, nfe)

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Pangolin	Δ0.21	loss · gain 0.05 · not in the SpliceAI release · independent
Constraint at this position
Conservation	phyloP -2.1	GERP -5
Overall
CADD	13.54	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.00882% European (non-Finnish) · 104/1,178,812 alleles

Filtering AF 0.00741% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.00693%

Overall 0.00683% 110/1,610,012 alleles · very rare

Ancestry group	Frequency	1 in
European (non-Finnish)grpmax	0.00882%	11,335
African / African-American	0.00534%	18,728
Remaining individualsnot grpmax-eligible	0.00161%	62,228
Finnishnot grpmax-eligible	0.00159%	62,826

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.Arg233=
Coding: c.699G>T
MANE Select: NM_001330311
dbSNP: rs771135299
Type: single nucleotide variant
Location: chr1:1340410 (GRCh38)
Gene constraint: LOEUF 1.046 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 60.70 · 3 PDB
Residue 233: the 'disordered' region

Full DVL1 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Similar variants

DVL1 p.Arg233Leu Uncertain significance ★ ⚠ same residue
DVL1 p.Arg233Pro Conflicting classifications of pathogenicity ★ ⚠ same residue
DVL1 p.Arg233Trp Uncertain significance ★ ⚠ same residue
DVL1 p.Ala125Val Uncertain significance ★★ ⚠ same type
DVL1 p.Ala288Val Uncertain significance ★★ ⚠ same type
DVL1 p.Ala361Thr Uncertain significance ★★ ⚠ same type
DVL1 p.Ala368Val Uncertain significance ★★ ⚠ same type
DVL1 p.Ala667Pro 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/dvl1-p-arg233 (accessed [today's date]).

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