Hs00433318_cn

• Gene Symbol: CCDC158
• Assay Reference Genome Location: Chr.4:76351076 on build GRCh38
• Cytoband: 4q21.1

Target Gene Details

• Entrez Gene ID: 339965
• Gene Name: coiled-coil domain containing 158
• Gene Aliases: -
• Location: Chr.4:76313039-76421920 on Build GRCh38
• Assay Gene Location: Within Exon 23

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
CCDC158	NM_001042784.1	17	2737	NP_001036249.1
	XM_005262974.4	18	2864	XP_005263031.1
	XM_006714204.3	18	2864	XP_006714267.1
	XM_011531908.2	19	2968	XP_011530210.1
	XM_011531909.2	19	2984	XP_011530211.1
	XM_011531910.2	18	3445	XP_011530212.1
	XM_011531911.1	18	2828	XP_011530213.1
	XM_011531912.2	18	2724	XP_011530214.1
	XM_011531913.1	17	2752	XP_011530215.1
	XM_011531914.2	17	2821	XP_011530216.1
	XM_011531915.2	17	2712	XP_011530217.1
	XM_011531916.2	17	2646	XP_011530218.1
	XM_011531917.1	18	2689	XP_011530219.1
	XM_017008160.1	19	3478	XP_016863649.1
	XM_017008161.1	13	1929	XP_016863650.1
	AK098600.1	6	754	BAC05347.1
	AK098636.1			BAC05359.1
	AL832445.1	6	2410
	BC086869.1	13	2107	AAH86869.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv2759262	Chr.4:76343443 - 76534252 on Build GRCh38	Loss	SHROOM3 CCDC158

More Information

Additional Information:

For this assay, SNP(s) [rs114770535] 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, DGV Variation