Hs03743965_cn

• Gene Symbol: FAM45A
• Assay Reference Genome Location: Chr.10:119114092 on build GRCh38
• Cytoband: 10q26.11

Target Gene Details

• Entrez Gene ID: 404636
• Gene Name: family with sequence similarity 45 member A
• Gene Aliases: -
• Location: Chr.10:119104065-119137984 on Build GRCh38
• Assay Gene Location: Within Intron 4

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM45A	NM_001303111.1			NP_001290040.1
	NM_001303112.1			NP_001290041.1
	NM_001303113.1			NP_001290042.1
	NM_207009.3			NP_996892.1
	NR_130122.1
	XM_006717849.3			XP_006717912.1
	XM_006717850.3			XP_006717913.1
	XM_006717851.3			XP_006717914.1
	XM_006717852.3			XP_006717915.1
	XM_017016261.1			XP_016871750.1
	XM_017016262.1			XP_016871751.1
	XM_017016263.1			XP_016871752.1
	XM_017016264.1			XP_016871753.1
	XM_017016265.1			XP_016871754.1
	XM_017016266.1			XP_016871755.1
	XM_017016267.1			XP_016871756.1
	AK000031.1			BAA90894.1
	AK027029.1
	AK293136.1
	AK293365.1
	AK297633.1
	AK297971.1
	BC022271.1			AAH22271.1
	BI753197.1
	DA531569.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv552214	Chr.10:119100409 - 119209705 on Build GRCh38	Loss	FAM45A PRDX3 SFXN4 GRK5
nsv1041093	Chr.10:118689033 - 119198373 on Build GRCh38	Gain	EIF3A FAM45A PRDX3 CACUL1 NANOS1 SNORA19 SFXN4

More Information

Additional Information:

For this assay, SNP(s) [rs79514881] 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