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BUB1 p.Gly20=

c.60C>G · rs1167761031 · VCV1751593

Likely benign Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
very rare (popmax 6.84e-05%)

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Splicing
SpliceAI<0.2all four deltas below 0.2 · G>A here scores Δ0.56 · evaluated, not missing
Constraint at this position
ConservationphyloP -3
Overall
CADD0.586PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes
Grpmax group 6.84e-05%
Overall 6.84e-05% 1/1,461,764 alleles · very rare

Rarity supports pathogenicity (ACMG PM2); frequency above a disease-specific BA1/BS1 threshold argues against it. A variant frequent in one ancestry group can be near-absent in others, so a single global figure can mislead.

Variant & gene context

Gene
BUB1
Protein
p.Gly20=
Coding
c.60C>G
MANE Select
NM_004336
dbSNP
rs1167761031
Type
single nucleotide variant
Location
chr2:110674332 (GRCh38)
Gene constraint
LOEUF 0.727 · pLI <0.01 (gnomAD)
Structure
AlphaFold pLDDT 63.91 · 11 PDB
Residue 20
the bub1 n-terminal domain; the 'necessary for kinetochore localization' region; a UniProt-annotated variant site (in)
Full BUB1 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Similar variants

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/bub1-p-gly20 (accessed [today's date]).

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