Hs02922712_cn

• Gene Symbol: FAM198B
• Assay Reference Genome Location: Chr.4:158125018 on build GRCh38
• Cytoband: 4q32.1

Target Gene Details

• Entrez Gene ID: 51313
• Gene Name: family with sequence similarity 198 member B
• Gene Aliases: AD021, AD036, C4orf18
• Location: Chr.4:158124580-158173050 on Build GRCh38
• Assay Gene Location: Within Exon 7

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM198B	NM_001031700.2	6	4380	NP_001026870.2
	NM_001128424.1	5	4356	NP_001121896.1
	NM_016613.6	5	4401	NP_057697.2
	AF260333.1	1	1842	AAG44664.1
	AK095474.1	1	1802
	AL832589.1	5	4227
	AL834177.1	5	3852	CAD38874.1
	BC017701.1	4	3304	AAH17701.1
	BC043193.2	6	4380	AAH43193.1
	BC100016.1	4	3240	AAI00017.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv1021067	Chr.4:158051130 - 158254323 on Build GRCh38	Gain	TMEM144 FAM198B

More Information

Additional Information:

For this assay, SNP(s) [rs145066523] 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