Hs03807264_cn

• Gene Symbol: CFAP73
• Assay Reference Genome Location: Chr.12:113152848 on build GRCh38
• Cytoband: 12q24.13

Target Gene Details

• Entrez Gene ID: 387885
• Gene Name: cilia and flagella associated protein 73
• Gene Aliases: CCDC42B, MIA2
• Location: Chr.12:113149162-113159276 on Build GRCh38
• Assay Gene Location: Within Exon 3

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
CFAP73	NM_001144872.1	3	228	NP_001138344.1
	XM_011538327.2	3	924	XP_011536629.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv519540	Chr.12:113042705 - 113459599 on Build GRCh38	Gain+Loss	SLC8B1 PLBD2 DDX54 TPCN1 MIR7106 SDSL SDS MIR6762 RASAL1 RITA1 CFAP73 IQCD DTX1
dgv2884n54	Chr.12:113115603 - 113166364 on Build GRCh38	Loss	RASAL1 DDX54 MIR7106 CFAP73
esv3892265	Chr.12:113099321 - 113527932 on Build GRCh38	Gain	SLC8B1 LHX5 PLBD2 DDX54 TPCN1 MIR7106 SDSL SDS MIR6762 RASAL1 LHX5-AS1 RITA1 CFAP73 IQCD
esv3630792	Chr.12:112988703 - 113838810 on Build GRCh38	Gain	SLC8B1 LHX5 RBM19 PLBD2 LINC01234 DDX54 TPCN1 MIR7106 SDSL SDS MIR6762 RASAL1 LHX5-AS1 RITA1 CFAP73 OAS2 IQCD DTX1

More Information

Additional Information:

For this assay, SNP(s) [rs116586136] 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