Is NHS p.Pro1129= (c.3387G>A) pathogenic?

NHS p.Pro1129= (c.3387G>A) is classified Likely benign in NHS (ClinVar, Single submitter, 1 submitter; last evaluated 2023-12-27). Very rare (popmax 0.000782%, nfe); Associated with Nance-Horan syndrome.

What condition is associated with NHS p.Pro1129= (c.3387G>A)?

NHS p.Pro1129= (c.3387G>A) is associated with Nance-Horan syndrome (ClinVar).

How common is NHS p.Pro1129= (c.3387G>A) in the general population?

NHS p.Pro1129= (c.3387G>A) is very rare (popmax 0.000782%, nfe) (gnomAD).

NHS p.Pro1129=

c.3387G>A · rs2066455694 · VCV1924769

Likely benign Single submitter

Classification

Likely benign

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

gnomAD v4.1

Rare

very rare (popmax 0.000782%, nfe)

Conditions

Nance-Horan syndrome

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 -5.2	GERP -5.9
Overall
CADD	0.159	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.000782% European (non-Finnish) · 7/894,896 alleles

Filtering AF 0.000325% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.000209%

Overall 0.000578% 7/1,210,903 alleles · very rare exomes 7/1,097,550 · genomes 0/113,353 · joint denominator

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: NHS
Protein: p.Pro1129=
Coding: c.3387G>A
MANE Select: NM_001291867
dbSNP: rs2066455694
Type: single nucleotide variant
Location: chrX:17727493 (GRCh38)
Structure: AlphaFold pLDDT 43.65

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

Disease context

Nance-Horan syndrome — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Similar variants

NHS p.Pro1129Ala Conflicting classifications of pathogenicity ★ same residue
NHS p.Pro1129Gln Uncertain significance ★ same residue
NHS p.Arg248Ter Pathogenic ★★ same condition
NHS p.Arg394Ter Pathogenic ★★ same condition
NHS p.Arg900Ter Pathogenic ★★ same condition
NHS p.Gln411Ter Pathogenic ★★ same condition
NHS p.Gln80Ter Pathogenic/Likely pathogenic ★★ same condition
NHS p.Ala564Val 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/nhs-p-pro1129 (accessed [today's date]).

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