Hs06199275_cn

• Gene Symbol: FAM49B
• Assay Reference Genome Location: Chr.8:129839837 on build GRCh38
• Cytoband: 8q24.21

Target Gene Details

• Entrez Gene ID: 51571
• Gene Name: family with sequence similarity 49 member B
• Gene Aliases: BM-009, L1
• Location: Chr.8:129839593-130016697 on Build GRCh38
• Assay Gene Location: Within Exon 19

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM49B	NM_001256763.1	13	3681	NP_001243692.1
	NM_016623.4	12	3594	NP_057707.3
	NR_046359.1	15	3947
	NR_046360.1	15	3857
	NR_046361.1	14	3847

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv3576607	Chr.8:129779957 - 129839982 on Build GRCh38	Gain	FAM49B GSDMC

More Information

Additional Information:

For this assay, SNP(s) [rs115949023] 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

Gene Ontology Categories:

Function(s)

protein binding