{{Rsnum
|rsid=2643103
|Gene=BCAS3
|Chromosome=17
|position=60709264
|Orientation=plus
|ReferenceAllele=A
|MissenseAllele=G
|GMAF=0.2153
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=BCAS3
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 0.0 | 100.0
| HCB | 0.7 | 16.8 | 82.5
| JPT | 0.0 | 24.8 | 75.2
| YRI | 67.3 | 25.9 | 6.8
| ASW | 36.8 | 49.1 | 14.0
| CHB | 0.7 | 16.8 | 82.5
| CHD | 0.9 | 13.8 | 85.3
| GIH | 2.0 | 11.0 | 87.0
| LWK | 69.1 | 29.1 | 1.8
| MEX | 0.0 | 5.4 | 94.6
| MKK | 55.1 | 40.4 | 4.5
| TSI | 0.0 | 2.0 | 98.0
| HapMapRevision=28
}}

{{Venter SNP
|rsid=2643103
|allele=G
|frequency=1
|uid=1103645356521
|type=homozygous_SNP
|hugo=BCAS3
|ensembl gene=ENSG00000141376
|ensembl transcript=ENST00000360207
|sift=TOLERATED
|disease=A chromosomal aberration involving BCAS3 may be a cause of breast cancer. Translocation t(17;20)(q23;q13) with BCAS4.
}}

{{GET Evidence
|gene=BCAS3
|aa_change=Asn87Ser
|aa_change_short=N87S
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2643103
|overall_frequency_n=7826
|overall_frequency_d=9716
|overall_frequency=0.805476
|n_genomes=47
|n_genomes_annotated=0
|n_haplomes=81
|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 | Illumina Human 1M}}