BRIP1 p.Pro787fs
c.2358del · VCV3482443
Pathogenic
Multiple submitters
Classification
Pathogenic
ClinVar
Review
Multiple submitters ★★☆☆
ClinVar · 2 submitters
Consequence
frameshift
predicted LoF
gnomAD v4.1
Rare
Conditions
3
Fanconi anemia complementation group J
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 haploinsufficient gene (ClinGen) |
|---|---|---|
| NMD | predicted | premature termination codon in exon 16 of 20 |
| Splicing | ||
| SpliceAI | — | not assessed · substitutions only |
| Constraint at this position | ||
| Conservation | phyloP 12 | GERP 2.1, phastCons 1 |
Predicted loss-of-function is descriptive, not an applied PVS1 code.
Variant & gene context
- Gene
- BRIP1
- Protein
- p.Pro787fs
- Coding
- c.2358del
- MANE Select
- NM_032043
- Type
- Deletion
- Location
- chr17:61743034 (GRCh38)
- Gene constraint
- LOEUF 0.848 · pLI <0.01 · ClinGen HI 3/3 (gnomAD)
- Structure
- AlphaFold pLDDT 64.19 · 6 PDB
Similar variants
- BRIP1 p.Pro787Arg Uncertain significance ★★ ⚠ same residue
- BRIP1 p.Pro787Leu Uncertain significance ★ ⚠ same residue
- BRIP1 p.Pro787Ser Uncertain significance ★ ⚠ same residue
- BRIP1 p.Pro787= Likely benign ★ same residue
- BRIP1 c.1629-3_1634del Likely pathogenic ★★ same condition
- BRIP1 c.1936del Pathogenic ★★ same condition
- BRIP1 c.205+1del Pathogenic/Likely pathogenic ★★ same condition
- BRIP1 c.2257+2_2257+8del 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/brip1-p-pro787fs (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown