Hs00193827_cn

• Gene Symbol: FAM69A
• Assay Reference Genome Location: Chr.1:92847266 on build GRCh38
• Cytoband: 1p22.1

Target Gene Details

• Entrez Gene ID: 388650
• Gene Name: family with sequence similarity 69 member A
• Gene Aliases: -
• Location: Chr.1:92832729-92961522 on Build GRCh38
• Assay Gene Location: Within Exon 5

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM69A	NM_001006605.4	4	484	NP_001006606.2
	NM_001252269.1	3	349	NP_001239198.1
	NM_001252270.1			NP_001239199.1
	NM_001252271.1	4	527	NP_001239200.1
	NM_001252273.1	4	484	NP_001239202.1
	AK027146.1
	AK303700.1	3	502
	AL536469.3	4	428
	AL702320.1	4	448
	BC070342.1	4	418	AAH70342.1
	BF979329.1
	DA141589.1	4	497
	DA155419.1	4	401
	DA348631.1
	DA736826.1	3	225
	DB199113.1	3	275
	DB475309.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv508393	Chr.1:92824956 - 92879367 on Build GRCh38	Deletion	SNORA66 RPL5 SNORD21 FAM69A
esv2714684	Chr.1:91095800 - 93049130 on Build GRCh38	Deletion	HSP90B3P RPAP2 TGFBR3 BRDT SNORD21 HFM1 SNORA66 GFI1 BTBD8 EPHX4 RPL5 SETSIP KIAA1107 C1orf146 GLMN EVI5 FAM69A CDC7
nsv1008602	Chr.1:92711254 - 93175251 on Build GRCh38	Gain	SNORA66 RPL5 TMED5 MTF2 SNORD21 EVI5 FAM69A

More Information

• Set Membership: Intragenic, Exonic, DGV Variation