Hs04880099_cn

• Gene Symbol: FAM149A
• Assay Reference Genome Location: Chr.4:186106060 on build GRCh38
• Cytoband: 4q35.1

Target Gene Details

• Entrez Gene ID: 25854
• Gene Name: family with sequence similarity 149 member A
• Gene Aliases: MST119, MSTP119
• Location: Chr.4:186104798-186172663 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM149A	XM_017007996.1			XP_016863485.1
	XM_017007997.1			XP_016863486.1
	AK057166.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv3894090	Chr.4:186011626 - 186212421 on Build GRCh38	Gain	FAM149A CYP4V2 TLR3 FLJ38576
nsv470097	Chr.4:186010756 - 186210350 on Build GRCh38	Gain	FAM149A CYP4V2 TLR3 FLJ38576
nsv1031258	Chr.4:186058545 - 186139101 on Build GRCh38	Gain	FAM149A TLR3
nsv1028146	Chr.4:185582745 - 186417181 on Build GRCh38	Gain	F11 FAM149A F11-AS1 KLKB1 CYP4V2 TLR3 SORBS2 FLJ38576
nsv830172	Chr.4:186091611 - 186247270 on Build GRCh38	Loss	FAM149A KLKB1 CYP4V2 FLJ38576
dgv683n27	Chr.4:186008072 - 186210350 on Build GRCh38	Gain	FAM149A CYP4V2 TLR3 FLJ38576
nsv461864	Chr.4:186085652 - 186335850 on Build GRCh38	Gain	F11 FAM149A F11-AS1 KLKB1 CYP4V2 TLR3 FLJ38576
esv3603517	Chr.4:186008703 - 186213065 on Build GRCh38	Gain	FAM149A CYP4V2 TLR3 FLJ38576
dgv1052e214	Chr.4:186072002 - 186212619 on Build GRCh38	Gain	FAM149A CYP4V2 TLR3 FLJ38576
nsv596393	Chr.4:186103154 - 186108667 on Build GRCh38	Gain	FAM149A

More Information

Additional Information:

For this assay, SNP(s) [rs116670326,rs74904616] 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