Is PRRT2 p.Ser208= (c.624C>T) pathogenic?

PRRT2 p.Ser208= (c.624C>T) is classified Likely benign in PRRT2 (ClinVar, Single submitter, 1 submitter; last evaluated 2023-09-15). Very rare (popmax 0.00345%, amr); Associated with episodic kinesigenic dyskinesia.

What condition is associated with PRRT2 p.Ser208= (c.624C>T)?

PRRT2 p.Ser208= (c.624C>T) is associated with episodic kinesigenic dyskinesia (ClinVar).

How common is PRRT2 p.Ser208= (c.624C>T) in the general population?

PRRT2 p.Ser208= (c.624C>T) is very rare (popmax 0.00345%, amr) (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.Ser208=

c.624C>T · rs757448392 · VCV1125369

Likely benign Single submitter

Classification

Likely benign

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

gnomAD v4.1

Rare

very rare (popmax 0.00345%, amr)

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 -2.4	GERP -2.2
Overall
CADD	6.697	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.00345% Admixed American · 2/57,984 alleles

Filtering AF 0.000572% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.000214%

Overall 0.000695% 11/1,582,432 alleles · very rare exomes 11/1,430,800 · genomes 0/151,632 · joint denominator

Ancestry group	Frequency	1 in
Admixed Americangrpmax	0.00345%	28,992
South Asian	0.00223%	44,780
Remaining individualsnot grpmax-eligible	0.00164%	61,086
European (non-Finnish)	0.000519%	192,817

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.Ser208=
Coding: c.624C>T
MANE Select: NM_145239
dbSNP: rs757448392
Type: single nucleotide variant
Location: chr16:29813678 (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-ser208 (accessed [today's date]).

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