Hs02389229_cn

• Gene Symbol: FAM71F2
• Assay Reference Genome Location: Chr.7:128672349 on build GRCh38
• Cytoband: 7q32.1

Target Gene Details

• Entrez Gene ID: 346653
• Gene Name: family with sequence similarity 71 member F2
• Gene Aliases: FAM137B
• Location: Chr.7:128671628-128702262 on Build GRCh38
• Assay Gene Location: Within Exon 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM71F2	NM_001012454.5	1	84	NP_001012457.3
	NM_001128926.3	1	84	NP_001122398.1
	NM_001290254.1	1	66	NP_001277183.1
	NM_001290255.1	1	84	NP_001277184.1
	XM_011516128.2	1	66	XP_011514430.1
	XM_011516129.2	1	66	XP_011514431.1
	XM_011516130.2	1	66	XP_011514432.1
	XM_011516131.2	1	66	XP_011514433.1
	XM_011516132.2	1	66	XP_011514434.1
	XM_011516135.2			XP_011514437.1
	XM_011516136.2			XP_011514438.1
	XM_017012147.1	1	84	XP_016867636.1
	XM_017012149.1	1	66	XP_016867638.1
	BC047310.1	1	56	AAH47310.2
	BC066973.1	1	58	AAH66973.2
	BC105729.1	1	57
	BC105730.1	1	57
	BC105731.1	1	57
	BI828876.1	1	64
	HY039605.1	1	85
	HY046252.1	1	67

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv2670312	Chr.7:128499519 - 128999613 on Build GRCh38	Deletion	CALU METTL2B CCDC136 ATP6V1F LINC01000 IRF5 KCP TNPO3 FAM71F1 LOC100130705 FLNC FAM71F2 OPN1SW
esv2735137	Chr.7:128499440 - 128999664 on Build GRCh38	Deletion	CALU METTL2B CCDC136 ATP6V1F LINC01000 IRF5 KCP TNPO3 FAM71F1 LOC100130705 FLNC FAM71F2 OPN1SW

More Information

Additional Information:

For this assay, SNP(s) [rs74343948] 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