Is AR p.Asp696Val (c.2087A>T) pathogenic?

AR p.Asp696Val (c.2087A>T) is classified Likely pathogenic in AR (ClinVar, Single submitter, 2 submitters; last evaluated 2022-03-04). AlphaMissense: likely pathogenic (0.9923); Absent from gnomAD v4.1; Associated with androgen insensitivity syndrome.

What condition is associated with AR p.Asp696Val (c.2087A>T)?

AR p.Asp696Val (c.2087A>T) is associated with androgen insensitivity syndrome, Kennedy disease (ClinVar).

How common is AR p.Asp696Val (c.2087A>T) in the general population?

AR p.Asp696Val (c.2087A>T) is absent from gnomAD v4.1 (gnomAD).

What do computational predictors say about AR p.Asp696Val (c.2087A>T)?

AlphaMissense predicts likely pathogenic (score 0.9923) — an in-silico prediction, not a clinical call.

AR p.Asp696Val

c.2087A>T · rs2147524993 · VCV2138585

Likely pathogenic Single submitter

Classification

Likely pathogenic

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 2 submitters

AlphaMissense

likely pathogenic

0.9923 · ACMG-weighted

gnomAD v4.1

Absent

absent from gnomAD v4.1

Missense predictors

3/3 damaging

AlphaMissense, REVEL, SaProt

Conditions

androgen insensitivity syndrome

Computational evidence

Protein change
AlphaMissense	0.9923	likely pathogenic ✓ concordant with ClinVar
REVEL	0.949	strongly pathogenic-leaning
SaProt	LLR -14.17	damaging
⇒ AlphaMissense, REVEL and SaProt all call this damaging.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 11	GERP 1.9, phastCons 1
Overall
CADD	26.5	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

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: AR
Protein: p.Asp696Val
Coding: c.2087A>T
MANE Select: NM_000044
dbSNP: rs2147524993
Type: single nucleotide variant
Location: chrX:67711603 (GRCh38)
Structure: AlphaFold pLDDT 58.85 · 95 PDB
Residue 696: the nr lbd domain; the 'interaction with ccar1' region; a UniProt-annotated variant site (in ais); the 'interaction with kat7' region; a UniProt-annotated variant site (in ais; almost complete loss of androgen binding and transcription activation); the 'interaction with lpxn' region

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

Disease context

androgen insensitivity syndrome — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Also linked: Kennedy disease

Similar variants

AR p.Asp696Asn Pathogenic ★★ same residue
AR c.1768+2T>C Pathogenic/Likely pathogenic ★★ same condition
AR c.1769-11T>A Pathogenic ★★ same condition
AR c.2450-6C>G Pathogenic ★★ same condition
AR p.Ala588Pro Pathogenic/Likely pathogenic ★★ same condition
AR p.Ala597Thr Pathogenic ★★ same condition
AR p.Ala688Val Pathogenic/Likely pathogenic ★★ same condition
AR p.Ala766Thr 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/ar-p-asp696val (accessed [today's date]).

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