Hs05739841_cn

• Gene Symbol: FAM163A
• Assay Reference Genome Location: Chr.1:179745068 on build GRCh38
• Cytoband: 1q25.2

Target Gene Details

• Entrez Gene ID: 148753
• Gene Name: family with sequence similarity 163 member A
• Gene Aliases: C1orf76, NDSP
• Location: Chr.1:179727763-179816198 on Build GRCh38
• Assay Gene Location: Within Intron 4

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM163A	NM_173509.2			NP_775780.1
	XM_005244913.2			XP_005244970.1
	XM_006711174.2			XP_006711237.1
	XM_006711175.2			XP_006711238.1
	XM_006711176.2			XP_006711239.1
	XM_006711177.1			XP_006711240.1
	XM_011509217.1			XP_011507519.1
	XM_011509221.1			XP_011507523.1
	XM_011509226.1			XP_011507528.1
	XM_011509228.1			XP_011507530.1
	XM_017000386.1			XP_016855875.1
	XM_017000387.1			XP_016855876.1
	XM_017000388.1			XP_016855877.1
	XM_017000389.1			XP_016855878.1
	XM_017000390.1			XP_016855879.1
	XM_017000391.1			XP_016855880.1
	XM_017000392.1			XP_016855881.1
	XM_017000393.1			XP_016855882.1
	AK292432.1
	AK302665.1
	AK310711.1
	AK313887.1
	AY902195.1			AAX07133.1
	BC009382.2			AAH09382.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv548339	Chr.1:179717109 - 179753692 on Build GRCh38	Gain	FAM163A
dgv64e214	Chr.1:179716874 - 179766076 on Build GRCh38	Gain	FAM163A

More Information

Additional Information:

For this assay, SNP(s) [rs74132249] 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