Hs04292037_cn

• Gene Symbol: FAM169A
• Assay Reference Genome Location: Chr.5:74795424 on build GRCh38
• Cytoband: 5q13.3

Target Gene Details

• Entrez Gene ID: 26049
• Gene Name: family with sequence similarity 169 member A
• Gene Aliases: SLAP75
• Location: Chr.5:74777574-74867994 on Build GRCh38
• Assay Gene Location: Within Intron 13

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM169A	NM_015566.2			NP_056381.1
	NR_046462.1
	XM_005248480.2			XP_005248537.1
	XM_011543306.2			XP_011541608.1
	XM_011543307.2			XP_011541609.1
	XM_017009332.1			XP_016864821.1
	XM_017009333.1			XP_016864822.1
	AB020695.1
	AK022981.1			BAB14344.1
	AK290004.1
	BX640902.1			CAE45948.1
	BX647536.1
	CR936791.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv598653	Chr.5:74697056 - 74799717 on Build GRCh38	Loss	NSA2 HEXB GFM2 FAM169A

More Information

Additional Information:

For this assay, SNP(s) [rs77948106,rs79646791] 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