BAP1 c.*644del
Likely pathogenic
Single submitter
Classification
Likely pathogenic
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
Conditions
1
BAP1-related tumor predisposition syndrome
Computational evidence
| Protein change | ||
| Missense predictors do not apply to this variant type; conservation carries the signal. | ||
| Splicing | ||
| SpliceAI | — | not assessed · substitutions only |
|---|---|---|
| Constraint at this position | ||
| Conservation | phyloP 2.4 | GERP -3.3, phastCons 1 |
Variant & gene context
- Gene
- BAP1
- Coding
- c.*644del
- MANE Select
- NM_007212 · reported on NM_004656
- Type
- Deletion
- Location
- chr3:52401644 (GRCh38)
- Structure
- AlphaFold pLDDT 78.27 · 28 PDB
Disease context
BAP1-related tumor predisposition syndrome — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatmentsFor BAP1-related tumor predisposition syndrome (Orphanet):
- Inheritance
- Autosomal dominant
- Onset
- Adult
Similar variants
- BAP1 c.123-10_129del Likely pathogenic ★★ same condition
- BAP1 c.1729+1del Pathogenic ★★ same condition
- BAP1 c.1984-3_1999del Likely pathogenic ★★ same condition
- BAP1 p.Ala138fs Pathogenic ★★ same condition
- BAP1 p.Arg207fs Pathogenic ★★ same condition
- BAP1 p.Arg518fs Pathogenic ★★ same condition
- BAP1 p.Asn363fs Pathogenic ★★ same condition
- BAP1 p.Asp400_Tyr401insTer 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-c-star-644del (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown