Hs05514550_cn

• Gene Symbol: FAM104A
• Assay Reference Genome Location: Chr.17:73220787 on build GRCh38
• Cytoband: 17q25.1

Target Gene Details

• Entrez Gene ID: 84923
• Gene Name: family with sequence similarity 104 member A
• Gene Aliases: -
• Location: Chr.17:73207353-73232394 on Build GRCh38
• Assay Gene Location: Within Intron 3

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM104A	NM_001098832.1			NP_001092302.1
	NM_001289410.1			NP_001276339.1
	NM_001289411.1			NP_001276340.1
	NM_001289412.1			NP_001276341.1
	NM_032837.2			NP_116226.2
	AK027681.1			BAB55292.1
	AK074755.1			BAC11183.1
	AK304556.1
	BC011054.1			AAH11054.1
	BC025238.1			AAH25238.1
	BG773537.1
	BX537858.1
	BX648968.1
	DB265439.1
	HY026689.1
	HY037907.1
	U92989.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv3641214	Chr.17:73220500 - 73221540 on Build GRCh38	Loss	FAM104A
esv2186746	Chr.17:73220352 - 73221660 on Build GRCh38	Deletion	FAM104A
esv2667654	Chr.17:73220483 - 73221544 on Build GRCh38	Deletion	FAM104A
nsv833534	Chr.17:73155642 - 73349355 on Build GRCh38	Loss	CPSF4L C17orf80 SSTR2 COG1 FAM104A SDK2 CDC42EP4
esv2562139	Chr.17:73220607 - 73222296 on Build GRCh38	Deletion	FAM104A

More Information

Additional Information:

For this assay, SNP(s) [rs139608939] 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

Gene Ontology Categories:

Function(s)

protein binding