Is BAP1 p.Gly591fs (c.1766_1767insTCAAT) pathogenic?

BAP1 p.Gly591fs (c.17661767insTCAAT) is classified Pathogenic in BAP1 (ClinVar, Single submitter, 1 submitter; last evaluated 2022-06-02). No gnomAD frequency available for this variant; Associated with hereditary neoplastic syndrome.

What condition is associated with BAP1 p.Gly591fs (c.1766_1767insTCAAT)?

BAP1 p.Gly591fs (c.1766_1767insTCAAT) is associated with hereditary neoplastic syndrome (ClinVar).

How common is BAP1 p.Gly591fs (c.1766_1767insTCAAT) in the general population?

BAP1 p.Gly591fs (c.1766_1767insTCAAT) is no gnomAD frequency available for this variant (gnomAD).

BAP1 p.Gly591fs

c.1766_1767insTCAAT · rs2471325616 · VCV1779671

Pathogenic Single submitter

Classification

Pathogenic

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

Consequence

frameshift

predicted LoF

gnomAD v4.1

Not reported

no gnomAD frequency available for this variant

Conditions

hereditary neoplastic syndrome

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Consequence	frameshift	predicted loss-of-function in a LoF-intolerant gene
NMD	predicted	premature termination codon in exon 14 of 17
Splicing
SpliceAI	—	not assessed · substitutions only
Constraint at this position
Conservation	phyloP 4.4	GERP -2.6, phastCons 1

Predicted loss-of-function is descriptive, not an applied PVS1 code.

Population frequency

dbSNP / gnomAD

No gnomAD frequency available for this variant. 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: BAP1
Protein: p.Gly591fs
Coding: c.1766_1767insTCAAT
MANE Select: NM_004656
dbSNP: rs2471325616
Type: Insertion
Location: chr3:52403261 (GRCh38)
Gene constraint: LOEUF 0.324 · pLI 1.00 (gnomAD)
Structure: AlphaFold pLDDT 63.87 · 4 PDB
Residue 591: a UniProt-annotated variant site (in tpds1); the 'disordered' region

Full BAP1 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

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

Similar variants

BAP1 p.Gly591= Benign/Likely benign ★★ same residue
BAP1 p.Ala258delinsTyrTer Pathogenic ★★ same condition
BAP1 p.Gly594fs Pathogenic ★★ same condition
BAP1 p.Ser571fs Pathogenic ★★ same condition
BAP1 c.68-2_68-1insTTCCTTTCCTTGACACCTTAAC Likely pathogenic ★ same condition
BAP1 p.Glu20fs Pathogenic ★ same condition
BAP1 p.Lys155fs Pathogenic ★ same condition
BAP1 p.Val174fs 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/bap1-p-gly591fs (accessed [today's date]).

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