Is PEX5 p.Pro16= (c.48G>A) pathogenic?

PEX5 p.Pro16= (c.48G>A) is classified Conflicting classifications of pathogenicity in PEX5 (ClinVar, Conflicting submitters, 4 submitters; last evaluated 2026-01-20). Ultra-rare (popmax 0.0142%, nfe); Associated with peroxisome biogenesis disorder 2B.

What condition is associated with PEX5 p.Pro16= (c.48G>A)?

PEX5 p.Pro16= (c.48G>A) is associated with peroxisome biogenesis disorder 2B (ClinVar).

How common is PEX5 p.Pro16= (c.48G>A) in the general population?

PEX5 p.Pro16= (c.48G>A) is ultra-rare (popmax 0.0142%, nfe) (gnomAD).

PEX5 p.Pro16=

c.48G>A · rs147958315 · VCV597925

Conflicting classifications of pathogenicity Conflicting submitters

Classification

Conflicting classifications of pathogenicity

ClinVar

Review

Conflicting submitters ★☆☆☆

ClinVar · 4 submitters

gnomAD v4.1

Rare

ultra-rare (popmax 0.0142%, nfe)

Conditions

peroxisome biogenesis disorder 2B

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 -0.32	GERP -2.7, phastCons 0.008
Overall
CADD	10.32	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.0142% European (non-Finnish) · 168/1,180,048 alleles

Filtering AF 0.0125% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.0118%

Overall 0.011% 178/1,614,102 alleles · ultra-rare exomes 171/1,461,874 · genomes 7/152,228 · joint denominator

Ancestry group	Frequency	1 in
European (non-Finnish)grpmax	0.0142%	7,024
Remaining individualsnot grpmax-eligible	0.0064%	15,623
Admixed American	0.005%	20,004
African / African-American	0.004%	24,981

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: PEX5
Protein: p.Pro16=
Coding: c.48G>A
MANE Select: NM_001351132
dbSNP: rs147958315
Type: single nucleotide variant
Location: chr12:7190425 (GRCh38)
Gene constraint: LOEUF 0.768 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 70.28 · 11 PDB
Residue 16: the 'amphipathic helix 1 (ah1)' region

Full PEX5 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

peroxisome biogenesis disorder 2B — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Similar variants

PEX5 c.449-2A>G Pathogenic/Likely pathogenic ★★ same condition
PEX5 c.552-1G>A Pathogenic/Likely pathogenic ★★ same condition
PEX5 c.847-2A>G Likely pathogenic ★★ same condition
PEX5 c.967-1G>A Likely pathogenic ★★ same condition
PEX5 p.Arg237Ter Pathogenic/Likely pathogenic ★★ same condition
PEX5 p.Arg276Ter Pathogenic/Likely pathogenic ★★ same condition
PEX5 p.Arg420Ter Pathogenic ★★ same condition
PEX5 p.Arg427Ter 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/pex5-p-pro16 (accessed [today's date]).

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