Is BGN p.His167= (c.501C>T) pathogenic?

BGN p.His167= (c.501C>T) is classified Likely benign in BGN (ClinVar, Multiple submitters, 2 submitters; last evaluated 2025-04-17). Ultra-rare (popmax 0.0174%, afr); Associated with Cardiovascular phenotype.

What condition is associated with BGN p.His167= (c.501C>T)?

BGN p.His167= (c.501C>T) is associated with Cardiovascular phenotype (ClinVar).

How common is BGN p.His167= (c.501C>T) in the general population?

BGN p.His167= (c.501C>T) is ultra-rare (popmax 0.0174%, afr) (gnomAD).

BGN p.His167=

c.501C>T · rs782677854 · VCV1744811

Likely benign Multiple submitters

Classification

Likely benign

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 2 submitters

gnomAD v4.1

Rare

ultra-rare (popmax 0.0174%, afr)

Conditions

Cardiovascular phenotype

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 -2.9	GERP -4.1
Overall
CADD	1.723	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.0174% African / African-American · 10/57,319 alleles

Filtering AF 0.00939% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.0072%

Overall 0.0019% 23/1,210,413 alleles · ultra-rare exomes 18/1,098,074 · genomes 5/112,339 · joint denominator

Ancestry group	Frequency	1 in
African / African-Americangrpmax	0.0174%	5,732
South Asian	0.00352%	28,419
East Asian	0.00296%	33,780
Remaining individualsnot grpmax-eligible	0.0021%	47,601
European (non-Finnish)	0.00101%	99,481

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: BGN
Protein: p.His167=
Coding: c.501C>T
MANE Select: NM_001711
dbSNP: rs782677854
Type: single nucleotide variant
Location: chrX:153506012 (GRCh38)
Structure: AlphaFold pLDDT 85.72

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

Disease context

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

Similar variants

BGN p.His167Gln Uncertain significance ★★ ⚠ same residue
BGN c.909+4A>G Uncertain significance ★★ same condition
BGN p.Ala330Asp Uncertain significance ★★ ⚠ same condition
BGN p.Ala330Pro Uncertain significance ★★ ⚠ same condition
BGN p.Ala41Ser Uncertain significance ★★ ⚠ same condition
BGN p.Ala44Thr Uncertain significance ★★ ⚠ same condition
BGN p.Arg106His Uncertain significance ★★ ⚠ same condition
BGN p.Arg170Cys 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/bgn-p-his167 (accessed [today's date]).

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