BGN p.Ser294=
c.882A>G · VCV4726341
Likely benign
Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Not reported
no allele count reported in gnomAD v4.1 (AN 1,204,540)
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 -4.6 | GERP -4.1 |
| Overall | ||
| CADD | 0.26 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
No allele count reported in gnomAD v4.1 (AN 1,204,540). 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
- BGN
- Protein
- p.Ser294=
- Coding
- c.882A>G
- MANE Select
- NM_001711
- Type
- single nucleotide variant
- Location
- chrX:153507158 (GRCh38)
- Structure
- AlphaFold pLDDT 85.72
Similar variants
- BGN c.770+1G>A Likely pathogenic ★★ same type
- BGN p.Gln75Ter Pathogenic/Likely pathogenic ★★ same type
- BGN p.Trp25Ter Likely pathogenic ★★ same type
- BGN c.909+4A>G Uncertain significance ★★ same type
- BGN p.Ala330Asp Uncertain significance ★★ ⚠ same type
- BGN p.Ala330Pro Uncertain significance ★★ ⚠ same type
- BGN p.Ala41Ser Uncertain significance ★★ ⚠ same type
- BGN p.Ala44Thr Uncertain significance ★★ ⚠ same type
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-ser294 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown