Is PRRT2 p.Pro204= (c.612C>G) pathogenic?

PRRT2 p.Pro204= (c.612C>G) is classified Benign/Likely benign in PRRT2 (ClinVar, Multiple submitters, 7 submitters; last evaluated 2026-01-15). Rare (popmax 0.391%, afr); Associated with episodic kinesigenic dyskinesia.

What condition is associated with PRRT2 p.Pro204= (c.612C>G)?

PRRT2 p.Pro204= (c.612C>G) is associated with episodic kinesigenic dyskinesia (ClinVar).

How common is PRRT2 p.Pro204= (c.612C>G) in the general population?

PRRT2 p.Pro204= (c.612C>G) is rare (popmax 0.391%, afr) (gnomAD).

How is Paroxysmal kinesigenic dyskinesia inherited?

Typically Autosomal dominant, Not applicable (Orphanet). A genetic counselor can assess individual risk for a family.

PRRT2 p.Pro204=

c.612C>G · rs149260055 · VCV138814

Benign/Likely benign Multiple submitters

Classification

Benign/Likely benign

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 7 submitters

gnomAD v4.1

Rare

rare (popmax 0.391%, afr)

Conditions

episodic kinesigenic dyskinesia

⚠ Built without this gene's context — gene constraint and dosage, protein structure, pathways, panels and related-variant links were not looked up for this page. why

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Splicing
SpliceAI	—	not looked up on this page · why
Constraint at this position
Conservation	phyloP -0.15	GERP -2.5, phastCons 0.45
Overall
CADD	2.831	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.391% African / African-American · 292/74,760 alleles

Filtering AF 0.354% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.339%

Overall 0.0203% 327/1,608,984 alleles · rare exomes 143/1,456,764 · genomes 184/152,220 · joint denominator

Ancestry group	Frequency	1 in
African / African-Americangrpmax	0.391%	256
Admixed American	0.0304%	3,293
Remaining individualsnot grpmax-eligible	0.0257%	3,884
European (non-Finnish)	8.49e-05%	1,177,544

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: PRRT2
Protein: p.Pro204=
Coding: c.612C>G
MANE Select: NM_145239
dbSNP: rs149260055
Type: single nucleotide variant
Location: chr16:29813666 (GRCh38)

Full PRRT2 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

episodic kinesigenic dyskinesia — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

For Paroxysmal kinesigenic dyskinesia (Orphanet):

Inheritance: Autosomal dominant, Not applicable
Onset: Adolescent, Adult, Childhood, Infancy
Prevalence: 1-9 / 1 000 000 (Worldwide)

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/prrt2-p-pro204 (accessed [today's date]).

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