Is PRX p.Pro694= (c.2082C>G) pathogenic?

PRX p.Pro694= (c.2082C>G) is classified Likely benign in PRX (ClinVar, Single submitter, 1 submitter; last evaluated 2023-02-17). Very rare (popmax 0.00682%, eas); Associated with Charcot-Marie-Tooth disease type 4.

What condition is associated with PRX p.Pro694= (c.2082C>G)?

PRX p.Pro694= (c.2082C>G) is associated with Charcot-Marie-Tooth disease type 4 (ClinVar).

How common is PRX p.Pro694= (c.2082C>G) in the general population?

PRX p.Pro694= (c.2082C>G) is very rare (popmax 0.00682%, eas) (gnomAD).

PRX p.Pro694=

c.2082C>G · rs1256959994 · VCV1660753

Likely benign Single submitter

Classification

Likely benign

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

gnomAD v4.1

Rare

very rare (popmax 0.00682%, eas)

Conditions

Charcot-Marie-Tooth disease type 4

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 -14	GERP -3.8
Overall
CADD	0.708	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.00682% East Asian · 3/43,992 alleles

Filtering AF 0.00195% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.00111%

Overall 0.000752% 12/1,595,032 alleles · very rare exomes 0/1,458,664 · genomes 12/136,368 · joint denominator

Ancestry group	Frequency	1 in
East Asiangrpmax	0.00682%	14,664
African / African-American	0.00577%	17,331
Finnishnot grpmax-eligible	0.00483%	20,712
Remaining individualsnot grpmax-eligible	0.00161%	61,958
European (non-Finnish)	8.53e-05%	1,172,750

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: PRX
Protein: p.Pro694=
Coding: c.2082C>G
MANE Select: NM_181882
dbSNP: rs1256959994
Type: single nucleotide variant
Location: chr19:40396270 (GRCh38)
Gene constraint: LOEUF 1.321 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 35.74 · 1 PDB
Residue 694: the '55 x 5 aa approximate tandem repeats of [lvmag]-[psreqc]-[edkl]-[livmap]-[aqkhrpe]; that may have a tripeptide spacer of [lv]-p-[ker]' region

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

Disease context

Charcot-Marie-Tooth disease type 4 — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Similar variants

PRX c.184+2T>C Likely pathogenic ★★ same condition
PRX p.Arg1070Ter Pathogenic/Likely pathogenic ★★ same condition
PRX p.Arg196Ter Pathogenic/Likely pathogenic ★★ same condition
PRX p.Arg364Ter Pathogenic ★★ same condition
PRX p.Arg368Ter Pathogenic/Likely pathogenic ★★ same condition
PRX p.Arg392Ter Pathogenic/Likely pathogenic ★★ same condition
PRX p.Arg464Ter Pathogenic/Likely pathogenic ★★ same condition
PRX p.Arg897Ter Pathogenic/Likely pathogenic ★★ 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/prx-p-pro694 (accessed [today's date]).

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