Hs07005484_cn

• Gene Symbol: FAM222A
• Assay Reference Genome Location: Chr.12:109721713 on build GRCh38
• Cytoband: 12q24.11

Target Gene Details

• Entrez Gene ID: 84915
• Gene Name: family with sequence similarity 222 member A
• Gene Aliases: C12orf34
• Location: Chr.12:109714382-109770509 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM222A	NM_032829.2			NP_116218.2
	DN994281.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv560133	Chr.12:109712747 - 109732223 on Build GRCh38	Gain	FAM222A

More Information

Additional Information:

For this assay, SNP(s) [rs78482353] 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