Hs06688820_cn

• Gene Symbol: CHCHD6
• Assay Reference Genome Location: Chr.3:126717845 on build GRCh38
• Cytoband: 3q21.3

Target Gene Details

• Entrez Gene ID: 84303
• Gene Name: coiled-coil-helix-coiled-coil-helix domain containing 6
• Gene Aliases: CHCM1, Mic25, PPP1R23
• Location: Chr.3:126704220-126960420 on Build GRCh38
• Assay Gene Location: Within Intron 2

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
CHCHD6	NM_001320610.1			NP_001307539.1
	NM_032343.2			NP_115719.1
	XM_011513234.1			XP_011511536.1
	XM_011513235.2			XP_011511537.1
	XM_017007320.1			XP_016862809.1
	XM_017007321.1			XP_016862810.1
	XM_017007322.1			XP_016862811.1
	AK310910.1
	AK311056.1
	BC006123.1			AAH06123.1
	DN992600.1
	JF264889.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv829718	Chr.3:126629911 - 126809810 on Build GRCh38	Gain	NUP210P1 CHCHD6 TXNRD3

More Information

Additional Information:

For this assay, SNP(s) [rs114405882] 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)

cellular response to DNA damage stimulus
cristae formation

Function(s)

protein binding