Hs03709215_cn

• Gene Symbol: SLC25A25-AS1
• Assay Reference Genome Location: Chr.9:128115674 on build GRCh38
• Cytoband: 9q34.11

Target Gene Details

• Entrez Gene ID: 100289019
• Gene Name: SLC25A25 antisense RNA 1
• Gene Aliases: -
• Location: Chr.9:128111171-128118734 on Build GRCh38
• Assay Gene Location: Within Intron 2

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
SLC25A25-AS1	NR_033374.1
	AK124723.1
	AL833509.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv951769	Chr.9:128101422 - 128129321 on Build GRCh38	Deletion	PTGES2 PTGES2-AS1 SLC25A25-AS1 SLC25A25
nsv615383	Chr.9:128091848 - 128128781 on Build GRCh38	Loss	PTGES2 PTGES2-AS1 SLC25A25-AS1 SLC25A25
nsv6723	Chr.9:128106647 - 128141731 on Build GRCh38	Deletion	PTGES2 PTGES2-AS1 SLC25A25-AS1 SLC25A25
nsv818724	Chr.9:128100434 - 128128781 on Build GRCh38	Loss	PTGES2 PTGES2-AS1 SLC25A25-AS1 SLC25A25
nsv471324	Chr.9:128039877 - 128130666 on Build GRCh38	Gain	PTGES2 PTGES2-AS1 SLC25A25-AS1 NAIF1 SLC25A25

More Information

Additional Information:

For this assay, SNP(s) [rs112560343] 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