Hs01867742_cn

• Gene Symbol: FAM117A
• Assay Reference Genome Location: Chr.17:49711376 on build GRCh38
• Cytoband: 17q21.33

Target Gene Details

• Entrez Gene ID: 81558
• Gene Name: family with sequence similarity 117 member A
• Gene Aliases: -
• Location: Chr.17:49710325-49764156 on Build GRCh38
• Assay Gene Location: Within Exon 9

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM117A	NM_030802.3	8	1310	NP_110429.1
	XM_017025182.1	8	2068	XP_016880671.1
	AF123073.1	8	1271	AAK01477.1
	AK302376.1	8	1124
	BC037572.1	8	1322	AAH37572.1
	BC065199.1	8	1275	AAH65199.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv525469	Chr.17:49704315 - 49720153 on Build GRCh38	Gain	FAM117A SLC35B1

More Information

Additional Information:

For this assay, SNP(s) [rs114334999] 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