Is PEX10 p.Ala37= (c.111G>T) pathogenic?

PEX10 p.Ala37= (c.111G>T) is classified Likely benign in PEX10 (ClinVar, Single submitter, 2 submitters; last evaluated 2025-04-30). Very rare (popmax 0.00685%, amr); Associated with Peroxisome biogenesis disorder, complementation group 7.

How common is PEX10 p.Ala37= (c.111G>T) in the general population?

PEX10 p.Ala37= (c.111G>T) is very rare (popmax 0.00685%, amr) (gnomAD).

PEX10 p.Ala37=

Q: What condition is associated with PEX10 p.Ala37= (c.111G>T)?

PEX10 p.Ala37= (c.111G>T) is associated with Peroxisome biogenesis disorder, complementation group 7, Zellweger spectrum disorders (ClinVar).

c.111G>T · rs1227962505 · VCV837587

Likely benign Single submitter

Classification

Likely benign

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 2 submitters

gnomAD v4.1

Rare

very rare (popmax 0.00685%, amr)

Conditions

Peroxisome biogenesis disorder, complementation group 7

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Splicing
SpliceAI	<0.2	no splice effect predicted · four deltas, not one · how we know
Constraint at this position
Conservation	phyloP -1.8	GERP -3.9
Overall
CADD	10.21	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.00685% Admixed American · 2/29,176 alleles

Filtering AF 0.00113% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.000424%

Overall 0.000216% 3/1,390,850 alleles · very rare exomes 3/1,238,542 · genomes 0/152,308 · joint denominator

Ancestry group	Frequency	1 in
Admixed Americangrpmax	0.00685%	14,588
Remaining individualsnot grpmax-eligible	0.00189%	52,980

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: PEX10
Protein: p.Ala37=
Coding: c.111G>T
MANE Select: NM_002617
dbSNP: rs1227962505
Type: single nucleotide variant
Location: chr1:2412392 (GRCh38)
Gene constraint: LOEUF 1.234 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 82.81

Full PEX10 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

Peroxisome biogenesis disorder, complementation group 7 — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Also linked: Zellweger spectrum disorders

Similar variants

PEX10 p.Ala37Glu Uncertain significance ★ ⚠ same residue
PEX10 c.113-1G>A Likely pathogenic ★★ same condition
PEX10 c.600+1G>A Pathogenic/Likely pathogenic ★★ same condition
PEX10 c.776+1G>A Likely pathogenic ★★ same condition
PEX10 c.776+1G>C Pathogenic/Likely pathogenic ★★ same condition
PEX10 c.776+2T>C Likely pathogenic ★★ same condition
PEX10 c.777-1G>A Likely pathogenic ★★ same condition
PEX10 c.912+1G>C 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/pex10-p-ala37 (accessed [today's date]).

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