Hs03923627_cn

• Gene Symbol: MAFTRR
• Assay Reference Genome Location: Chr.16:79737306 on build GRCh38
• Cytoband: 16q23.2

Target Gene Details

• Entrez Gene ID: 102467146
• Gene Name: MAF transcriptional regulator RNA
• Gene Aliases: linc-MAF-4, lincMAF4
• Location: Chr.16:79721312-79770532 on Build GRCh38
• Assay Gene Location: Within Intron 5

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
MAFTRR	NR_104663.1
	BX108785.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv3639248	Chr.16:79709018 - 79770282 on Build GRCh38	Loss	MAFTRR
esv3572208	Chr.16:79668676 - 80101641 on Build GRCh38	Gain	MAFTRR LINC01229
nsv833296	Chr.16:79658339 - 79855830 on Build GRCh38	Loss	MAFTRR LINC01229
nsv833297	Chr.16:79698604 - 79886522 on Build GRCh38	Gain	MAFTRR LINC01229
nsv573285	Chr.16:79124285 - 80093429 on Build GRCh38	Gain	WWOX LOC105371352 MAFTRR LINC01229 MAF

More Information

Additional Information:

For this assay, SNP(s) [rs76730528] 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, Intronic, Non-exonic, DGV Variation