Hs05517903_cn

• Gene Symbol: TMEM220-AS1
• Assay Reference Genome Location: Chr.17:10735983 on build GRCh38
• Cytoband: 17p13.1

Target Gene Details

• Entrez Gene ID: 101101775
• Gene Name: TMEM220 antisense RNA 1
• Gene Aliases: -
• Location: Chr.17:10729777-10815164 on Build GRCh38
• Assay Gene Location: Within Intron 2

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
TMEM220-AS1	NR_073455.1
	NR_073456.1
	NR_073457.1
	NR_073458.1
	BQ694074.1
	BQ694934.1
	DA035282.1
	DA190285.1
	DA747858.1
	DA867863.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv2675560	Chr.17:10710661 - 10748164 on Build GRCh38	Deletion	ADPRM MAGOH2P TMEM220-AS1 TMEM220
nsv1065819	Chr.17:10622619 - 10784575 on Build GRCh38	Gain	MYHAS ADPRM MAGOH2P TMEM220-AS1 MYH3 SCO1 TMEM220
esv3639941	Chr.17:10710674 - 10748133 on Build GRCh38	Loss	ADPRM MAGOH2P TMEM220-AS1 TMEM220
nsv833367	Chr.17:10683841 - 10826633 on Build GRCh38	Loss	ADPRM MAGOH2P TMEM220-AS1 PIRT SCO1 LINC00675 TMEM220
nsv1058835	Chr.17:10322963 - 10939602 on Build GRCh38	Loss	MYH2 MYH8 TMEM220-AS1 MYH13 SCO1 MYH1 MYHAS ADPRM MAGOH2P MYH3 PIRT MYH4 LINC00675 TMEM220

More Information

Additional Information:

For this assay, SNP(s) [rs117032088] 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