BUB3 p.Ser48=
c.144C>G · rs2493755541 · VCV1772886
Likely benign
Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Absent
absent from gnomAD v4.1
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 0.46 | GERP 0.62, phastCons 0.99 |
| Overall | ||
| CADD | 13.56 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Absent from gnomAD v4.1. Not observed in any sequenced alleles — a rarity signal (ACMG PM2-supporting), not evidence of pathogenicity on its own.
Variant & gene context
- Gene
- BUB3
- Protein
- p.Ser48=
- Coding
- c.144C>G
- MANE Select
- NM_004725
- dbSNP
- rs2493755541
- Type
- single nucleotide variant
- Location
- chr10:123155061 (GRCh38)
- Gene constraint
- LOEUF 0.77 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 96.10
Similar variants
- BUB3 p.Arg314= Likely benign ★★ same type
- BUB3 p.Ser197= Likely benign ★★ same type
- BUB3 p.Ser198= Likely benign ★★ same type
- BUB3 p.Ala131Val Uncertain significance ★ ⚠ same type
- BUB3 p.Ala155Val Uncertain significance ★ ⚠ same type
- BUB3 p.Ala187Gly Uncertain significance ★ ⚠ same type
- BUB3 p.Ala239Gly Uncertain significance ★ ⚠ same type
- BUB3 p.Ala292Val 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/bub3-p-ser48 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown