{{Rsnum
|rsid=1801376
|Gene=BUB1B
|Chromosome=15
|position=40185630
|Orientation=plus
|ReferenceAllele=A
|MissenseAllele=G
|GMAF=0.3774
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 55.8 | 36.3 | 8.0
| HCB | 10.9 | 43.1 | 46.0
| JPT | 8.8 | 53.1 | 38.1
| YRI | 78.2 | 20.4 | 1.4
| ASW | 70.2 | 29.8 | 0.0
| CHB | 10.9 | 43.1 | 46.0
| CHD | 15.6 | 39.4 | 45.0
| GIH | 37.6 | 52.5 | 9.9
| LWK | 64.5 | 30.0 | 5.5
| MEX | 37.9 | 48.3 | 13.8
| MKK | 38.5 | 46.2 | 15.4
| TSI | 43.1 | 50.0 | 6.9
| HapMapRevision=28
}}

{{Venter SNP
|rsid=1801376
|allele=A
|frequency=0.733
|uid=1103645592560
|type=homozygous_SNP
|hugo=BUB1B
|ensembl gene=ENSG00000156970
|ensembl transcript=ENST00000287598
|sift=TOLERATED
|disease=Defects in BUB1B are associated with tumor formation.
}}

{{GET Evidence
|gene=BUB1B
|aa_change=Arg349Gln
|aa_change_short=R349Q
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1801376
|overall_frequency_n=7919
|overall_frequency_d=10758
|overall_frequency=0.736103
|n_genomes=49
|n_genomes_annotated=0
|n_haplomes=79
|n_articles=0
|n_articles_annotated=0
|nblosum100=0
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}