Hs06968073_cn

• Gene Symbol: BRI3BP
• Assay Reference Genome Location: Chr.12:125026177 on build GRCh38
• Cytoband: 12q24.31

Target Gene Details

• Entrez Gene ID: 140707
• Gene Name: BRI3 binding protein
• Gene Aliases: BNAS1, HCCR-1, HCCR-2, HCCRBP-1, KG19
• Location: Chr.12:124993648-125051845 on Build GRCh38
• Assay Gene Location: Within Intron 3

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
BRI3BP	XM_011537940.2			XP_011536242.1
	AF284094.1	3	1590	AAL54382.1
	AK055703.1	1	1167

Target Gene Details

• Entrez Gene ID: 102659353
• Gene Name: TNF and HNRNPL related immunoregulatory long non-coding RNA
• Gene Aliases: BRI3BP-AS1, BRI3BPAS1, Linc1992, TCONS_00020260
• Location: Chr.12:125025443-125027423 on Build GRCh38
• Assay Gene Location: Within Exon 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
THRIL	NR_110375.1	1	1247
	AK025766.1	1	246

Target Copy Number Variation Details

• DGV Version: Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
nsv1051020	Chr.12:125015140 - 125809096 on Build GRCh38	Gain	TMEM132B BRI3BP THRIL AACS
nsv1047470	Chr.12:125009120 - 125044073 on Build GRCh38	Loss	BRI3BP THRIL
esv3631032	Chr.12:125022783 - 125033641 on Build GRCh38	Gain	BRI3BP THRIL
esv3892269	Chr.12:125024464 - 125055560 on Build GRCh38	Gain	BRI3BP THRIL

More Information

Additional Information:

For this assay, SNP(s) [rs73231614] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

• Set Membership: Intragenic, Exonic, Intronic, Non-exonic, DGV Variation