Is PEX19 p.Asp166Val (c.497A>T) pathogenic?

PEX19 p.Asp166Val (c.497A>T) is classified Uncertain significance in PEX19 (ClinVar, Single submitter, 1 submitter; last evaluated 2025-09-09). AlphaMissense: likely benign (0.1479); Absent from gnomAD v4.1; Associated with Inborn genetic diseases.

What condition is associated with PEX19 p.Asp166Val (c.497A>T)?

PEX19 p.Asp166Val (c.497A>T) is associated with Inborn genetic diseases (ClinVar).

How common is PEX19 p.Asp166Val (c.497A>T) in the general population?

PEX19 p.Asp166Val (c.497A>T) is absent from gnomAD v4.1 (gnomAD).

What do computational predictors say about PEX19 p.Asp166Val (c.497A>T)?

AlphaMissense predicts likely benign (score 0.1479) — an in-silico prediction, not a clinical call.

PEX19 p.Asp166Val

c.497A>T · VCV4134907

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

likely benign

0.1479 · ACMG-weighted

gnomAD v4.1

Absent

absent from gnomAD v4.1

Missense predictors

0/2 damaging

AlphaMissense, SaProt · REVEL indeterminate

Conditions

Inborn genetic diseases

Computational evidence

Protein change
AlphaMissense	0.1479	likely benign
REVEL	0.309	indeterminate
SaProt	LLR -7.91	tolerated
⇒ AlphaMissense and SaProt both call this tolerated; REVEL is indeterminate.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 4.2	GERP 1.4, phastCons 1
Regional constraint	o/e 1.08	unconstrained · MANE · 5,570 bp · p 0.15 · regional, not allelic
Overall
CADD	22.1	PHRED · no single calibrated threshold — expert panels disagree

ClinVar classifies this uncertain; the computational predictors unanimously lean tolerated — a triage signal, not a reclassification

AlphaMissense carries the ACMG weight for missense; REVEL and SaProt are independent agreement signals.

Population frequency

gnomAD v4.1 · exomes + genomes

Absent from gnomAD v4.1. Not observed in any sequenced alleles — a rarity signal (ACMG PM2-supporting), not evidence of pathogenicity on its own.

Variant & gene context

Gene: PEX19
Protein: p.Asp166Val
Coding: c.497A>T
MANE Select: NM_002857
Type: single nucleotide variant
Location: chr1:160282136 (GRCh38)
Gene constraint: LOEUF 1.066 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 71.95 · 5 PDB

Full PEX19 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

Inborn genetic diseases — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Similar variants

PEX19 p.Asp166Glu Conflicting classifications of pathogenicity ★ ⚠ same residue
PEX19 p.Ala14Pro Uncertain significance ★★ ⚠ same condition
PEX19 p.Ala37Val Uncertain significance ★★ ⚠ same condition
PEX19 p.Ala95Asp Uncertain significance ★★ ⚠ same condition
PEX19 p.Asp163Gly Uncertain significance ★★ ⚠ same condition
PEX19 p.Asp30Asn Uncertain significance ★★ ⚠ same condition
PEX19 p.Gln122Arg Uncertain significance ★★ ⚠ same condition
PEX19 p.Gln123Glu Uncertain significance ★★ ⚠ 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/pex19-p-asp166val (accessed [today's date]).

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