Hs03373802_cn

• Gene Symbol: TTC34
• Assay Reference Genome Location: Chr.1:2638637 on build GRCh38
• Cytoband: 1p36.32

Target Gene Details

• Entrez Gene ID: 100287898
• Gene Name: tetratricopeptide repeat domain 34
• Gene Aliases: -
• Location: Chr.1:2636988-2789737 on Build GRCh38
• Assay Gene Location: Within Exon 9

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
TTC34	XM_016999990.1	9	3997	XP_016855479.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv21805	Chr.1:2634485 - 2702743 on Build GRCh38	Gain+Loss	TTC34
nsv829648	Chr.1:2567689 - 2640901 on Build GRCh38	Loss	LOC100996583 FAM213B TTC34 MMEL1
nsv951593	Chr.1:2628062 - 2645961 on Build GRCh38	Deletion	TTC34 MMEL1
nsv428399	Chr.1:2622539 - 3235926 on Build GRCh38	Gain	MIR4251 ACTRT2 PRDM16 TTC34 LINC00982 MMEL1
nsv470684	Chr.1:2394570 - 2930923 on Build GRCh38	Loss	LOC100996583 PEX10 TNFRSF14 FAM213B LOC115110 PLCH2 TTC34 HES5 PANK4 RER1 MMEL1
nsv545083	Chr.1:2575976 - 2653099 on Build GRCh38	Gain	LOC100996583 FAM213B TTC34 MMEL1

More Information

Additional Information:

For this assay, SNP(s) [rs77891804] 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