Is ABCD1 p.Glu291Lys (c.871G>A) pathogenic?

ABCD1 p.Glu291Lys (c.871G>A) is classified Pathogenic in ABCD1 (ClinVar, Single submitter, 2 submitters; last evaluated 2024-10-24). AlphaMissense: likely pathogenic (0.9879); Absent from gnomAD v4.1; Associated with adrenoleukodystrophy.

What condition is associated with ABCD1 p.Glu291Lys (c.871G>A)?

ABCD1 p.Glu291Lys (c.871G>A) is associated with adrenoleukodystrophy (ClinVar).

How common is ABCD1 p.Glu291Lys (c.871G>A) in the general population?

ABCD1 p.Glu291Lys (c.871G>A) is absent from gnomAD v4.1 (gnomAD).

How is X-linked adrenoleukodystrophy inherited?

Typically X-linked dominant (Orphanet). A genetic counselor can assess individual risk for a family.

What do computational predictors say about ABCD1 p.Glu291Lys (c.871G>A)?

AlphaMissense predicts likely pathogenic (score 0.9879) — an in-silico prediction, not a clinical call.

ABCD1 p.Glu291Lys

c.871G>A · rs128624213 · VCV11292

Pathogenic Single submitter

Classification

Pathogenic

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 2 submitters

AlphaMissense

likely pathogenic

0.9879 · ACMG-weighted

gnomAD v4.1

Not reported

no allele count reported in gnomAD v4.1 (AN 1,166,804)

Missense predictors

3/3 damaging

AlphaMissense, REVEL, SaProt

Conditions

adrenoleukodystrophy

Computational evidence

Protein change
AlphaMissense	0.9879	likely pathogenic ✓ concordant with ClinVar · top 7% in ABCD1
REVEL	0.971	strongly pathogenic-leaning
SaProt	LLR -10.22	damaging
⇒ AlphaMissense, REVEL and SaProt all call this damaging.
Splicing
SpliceAI	<0.2	all four deltas below 0.2 · G>T here scores Δ0.33 · evaluated, not missing
Constraint at this position
Conservation	phyloP 12	GERP 1.7, phastCons 1
Regional constraint	o/e 0.69	unconstrained · MANE · 14 kb · p 4.8e-06 · regional, not allelic
Overall
CADD	32.0	PHRED · no single calibrated threshold — expert panels disagree

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

Population frequency

gnomAD v4.1 · exomes + genomes

No allele count reported in gnomAD v4.1 (AN 1,166,804). This is missing data, not an absence: the variant may or may not be present in gnomAD. Rarity (ACMG PM2) and BA1/BS1 cannot be assessed for it.

Variant & gene context

Gene: ABCD1
Protein: p.Glu291Lys
Coding: c.871G>A
MANE Select: NM_000033
dbSNP: rs128624213
Type: single nucleotide variant
Location: chrX:153726137 (GRCh38)
Structure: AlphaFold pLDDT 81.58 · 14 PDB
Residue 291: an α-helix; the abc transmembrane type-1 domain; a UniProt-annotated variant site (in ald; acald and cald-types); a UniProt-annotated variant site (in ald); a UniProt-annotated variant site (in ald; ald-type)

Full ABCD1 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

adrenoleukodystrophy — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

For X-linked adrenoleukodystrophy (Orphanet):

Inheritance: X-linked dominant
Onset: Adolescent, Adult, Childhood, Elderly
Prevalence: 1-9 / 1 000 000 (Israel)

Similar variants

ABCD1 p.Glu291Asp Pathogenic/Likely pathogenic ★★ same residue
ABCD1 p.Glu291Ala Pathogenic ★ same residue
ABCD1 p.Glu291Gly Likely pathogenic ★ same residue
ABCD1 c.1635-2A>G Pathogenic ★★ same condition
ABCD1 c.1781-1G>C Pathogenic ★★ same condition
ABCD1 c.1781-1G>T Pathogenic/Likely pathogenic ★★ same condition
ABCD1 c.1866-10G>A Pathogenic/Likely pathogenic ★★ same condition
ABCD1 c.1866-1G>C 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/abcd1-p-glu291lys (accessed [today's date]).

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