Hs05144325_cn

• Gene Symbol: FAM107B
• Assay Reference Genome Location: Chr.10:14534187 on build GRCh38
• Cytoband: 10p13

Target Gene Details

• Entrez Gene ID: 83641
• Gene Name: family with sequence similarity 107 member B
• Gene Aliases: C10orf45
• Location: Chr.10:14518557-14774897 on Build GRCh38
• Assay Gene Location: Within Intron 13

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM107B	NM_001282695.1			NP_001269624.1
	NM_001282696.1			NP_001269625.1
	NM_001282697.1			NP_001269626.1
	NM_001282698.1			NP_001269627.1
	NM_001282699.1			NP_001269628.1
	NM_001282700.1			NP_001269629.1
	NM_001282701.1			NP_001269630.1
	NM_001282702.1			NP_001269631.1
	NM_001282703.1			NP_001269632.1
	NM_001320735.1			NP_001307664.1
	NM_001320736.1			NP_001307665.1
	NM_001320737.1			NP_001307666.1
	NM_001320738.1			NP_001307667.1
	NM_001320739.1			NP_001307668.1
	NM_001320740.1			NP_001307669.1
	NM_031453.3			NP_113641.2
	XM_005252616.3			XP_005252673.1
	XM_011519735.1			XP_011518037.1
	XM_017016746.1			XP_016872235.1
	XM_017016747.1			XP_016872236.1
	XM_017016748.1			XP_016872237.1
	XM_017016749.1			XP_016872238.1
	AK127413.1			BAC86966.1
	AK289959.1
	AL136885.1			CAB66819.1
	BC064407.1			AAH64407.1
	BC072452.1			AAH72452.1
	BF979432.1
	DA116139.1
	DA269906.1
	DA305421.1
	DA340804.1
	DA390740.1
	DA409460.1
	DA412617.1
	DA543225.1
	DA813465.1
	DA954468.1
	DA962195.1
	DB194372.1
	DB198416.1
	DB240036.1
	DC327230.1
	DC332216.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv831791	Chr.10:14505865 - 14682240 on Build GRCh38	Gain	FAM107B
esv34151	Chr.10:14344296 - 14751833 on Build GRCh38	Loss	FAM107B MIR4293 MIR1265
nsv5877	Chr.10:14521492 - 14555125 on Build GRCh38	Insertion	FAM107B
nsv528028	Chr.10:14400348 - 14563663 on Build GRCh38	Gain	FAM107B MIR1265
nsv549997	Chr.10:14459237 - 14814109 on Build GRCh38	Gain	FAM107B
nsv437659	Chr.10:14521098 - 14560444 on Build GRCh38	Loss	FAM107B

More Information

Additional Information:

For this assay, SNP(s) [rs116571457] 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:

Process(es)

sensory perception of sound