PRX p.Arg1391=
c.4173G>A · rs983272464 · VCV2166282
Likely benign
Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
very rare (popmax 0.00871%, amr)
Conditions
1
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 0.05 | GERP -2.1, phastCons 0.002 |
| Overall | ||
| CADD | 1.833 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
0.00871%
Admixed American · 5/57,430 alleles
Filtering AF
0.00337%
ClinGen BA1/BS1 input
FAF95, joint · FAF99 0.00214%
Overall
0.000567%
9/1,587,614 alleles · very rare
exomes 5/1,435,430 · genomes 4/152,184 · joint denominator
| Ancestry group | Frequency | 1 in |
|---|---|---|
| Admixed Americangrpmax | 0.00871% | 11,486 |
| East Asian | 0.00225% | 44,470 |
| Remaining individualsnot grpmax-eligible | 0.00164% | 61,088 |
| European (non-Finnish) | 0.000172% | 582,076 |
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.Arg1391=
- Coding
- c.4173G>A
- MANE Select
- NM_181882
- dbSNP
- rs983272464
- Type
- single nucleotide variant
- Location
- chr19:40394179 (GRCh38)
- Gene constraint
- LOEUF 1.321 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 35.74 · 1 PDB
- Residue 1391
- the 'disordered' region
Similar variants
- PRX p.Arg1391Gln Uncertain significance ★★ ⚠ same residue
- PRX p.Arg1391Gly Uncertain significance ★★ ⚠ same residue
- PRX p.Arg1391Trp Uncertain significance ★★ ⚠ same residue
- PRX p.Arg1391Pro Uncertain significance ★ ⚠ same residue
- 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
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-arg1391 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown