Is BBS5 p.Val167= (c.501T>A) pathogenic?

BBS5 p.Val167= (c.501T>A) is classified Benign in BBS5 (ClinVar, Multiple submitters, 4 submitters; last evaluated 2026-01-31). Low-frequency (popmax 3.21%, afr); Associated with Bardet-Biedl syndrome.

What condition is associated with BBS5 p.Val167= (c.501T>A)?

BBS5 p.Val167= (c.501T>A) is associated with Bardet-Biedl syndrome (ClinVar).

How common is BBS5 p.Val167= (c.501T>A) in the general population?

BBS5 p.Val167= (c.501T>A) is low-frequency (popmax 3.21%, afr) (gnomAD).

How is Bardet-Biedl syndrome inherited?

Typically Autosomal recessive, Oligogenic (Orphanet). A genetic counselor can assess individual risk for a family.

BBS5 p.Val167=

c.501T>A · rs75690869 · VCV262637

Benign Multiple submitters

Classification

Benign

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 4 submitters

gnomAD v4.1

Rare

low-frequency (popmax 3.21%, afr)

Conditions

Bardet-Biedl 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 -0.061	GERP -3.8, phastCons 0.027
Overall
CADD	4.101	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 3.21% African / African-American · 2,406/75,026 alleles

Filtering AF 3.1% ClinGen BA1/BS1 input FAF95, joint · FAF99 3.06%

Overall 0.17% 2,740/1,613,694 alleles · low-frequency exomes 1,355/1,461,360 · genomes 1,385/152,334 · joint denominator

Ancestry group	Frequency	1 in
African / African-Americangrpmax	3.21%	31
Remaining individualsnot grpmax-eligible	0.243%	411
Admixed American	0.217%	462
Middle Eastern	0.0828%	1,208
South Asian	0.0187%	5,357
European (non-Finnish)	0.00254%	39,327

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: BBS5
Protein: p.Val167=
Coding: c.501T>A
MANE Select: NM_152384
dbSNP: rs75690869
Type: single nucleotide variant
Location: chr2:169492988 (GRCh38)
Gene constraint: LOEUF 0.884 · pLI <0.01 · ClinGen HI gene assoc. with recessive phenotype (gnomAD)
Structure: AlphaFold pLDDT 88.87 · 1 PDB

Full BBS5 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

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

For Bardet-Biedl syndrome (Orphanet):

Inheritance: Autosomal recessive, Oligogenic
Onset: Antenatal, Childhood, Infancy, Neonatal
Prevalence: 1-9 / 100 000 (Specific population)

Similar variants

BBS5 p.Val167Ile Uncertain significance ★ ⚠ same residue
BBS5 c.143-1G>C Pathogenic/Likely pathogenic ★★ same condition
BBS5 c.209-1G>A Pathogenic/Likely pathogenic ★★ same condition
BBS5 c.209-2A>G Likely pathogenic ★★ same condition
BBS5 c.522+3A>G Pathogenic/Likely pathogenic ★★ same condition
BBS5 c.681+1G>T Pathogenic/Likely pathogenic ★★ same condition
BBS5 p.Arg138Cys Likely pathogenic ★★ same condition
BBS5 p.Arg138His Pathogenic/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/bbs5-p-val167 (accessed [today's date]).

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