Is DRD2 p.Pro322= (c.966C>T) pathogenic?

DRD2 p.Pro322= (c.966C>T) is classified Likely benign in DRD2 (ClinVar, Single submitter, 1 submitter; last evaluated 2025-10-08). Rare (popmax 0.123%, nfe); Associated with dystonic disorder.

What condition is associated with DRD2 p.Pro322= (c.966C>T)?

DRD2 p.Pro322= (c.966C>T) is associated with dystonic disorder (ClinVar).

How common is DRD2 p.Pro322= (c.966C>T) in the general population?

DRD2 p.Pro322= (c.966C>T) is rare (popmax 0.123%, nfe) (gnomAD).

DRD2 p.Pro322=

c.966C>T · rs143935143 · VCV696320

Likely benign Single submitter

Classification

Likely benign

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

gnomAD v4.1

Rare

rare (popmax 0.123%, nfe)

Conditions

dystonic disorder

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
Constraint at this position
Conservation	phyloP -4.6	GERP -4.5
Overall
CADD	0.624	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.123% European (non-Finnish) · 1,452/1,179,948 alleles

Filtering AF 0.118% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.116%

Overall 0.0978% 1,578/1,613,960 alleles · rare exomes 1,509/1,461,778 · genomes 69/152,182 · joint denominator

Ancestry group	Frequency	1 in
European (non-Finnish)grpmax	0.123%	813
Remaining individualsnot grpmax-eligible	0.056%	1,785
Finnishnot grpmax-eligible	0.0437%	2,287
South Asian	0.0373%	2,679
African / African-American	0.0254%	3,944
Admixed American	0.01%	10,003
East Asian	0.00891%	11,220

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: DRD2
Protein: p.Pro322=
Coding: c.966C>T
MANE Select: NM_000795
dbSNP: rs143935143
Type: single nucleotide variant
Location: chr11:113412728 (GRCh38)
Gene constraint: LOEUF 0.372 · pLI 1.00 (gnomAD)
Structure: AlphaFold pLDDT 72.49 · 11 PDB
Residue 322: the 'interaction with ppp1r9b' region; the 'disordered' region

Full DRD2 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

dystonic disorder — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Similar variants

DRD2 p.Arg274Gln Uncertain significance ★★ ⚠ same condition
DRD2 p.Gln366Lys Uncertain significance ★★ ⚠ same condition
DRD2 p.Glu99Lys Uncertain significance ★★ ⚠ same condition
DRD2 p.Gly261Arg Uncertain significance ★★ ⚠ same condition
DRD2 p.His316Pro Uncertain significance ★★ ⚠ same condition
DRD2 p.Ile431Thr Uncertain significance ★★ ⚠ same condition
DRD2 p.Pro300His Uncertain significance ★★ ⚠ same condition
DRD2 c.1139-653A>C Benign ★★ 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/drd2-p-pro322 (accessed [today's date]).

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