Hs04525496_cn

• Gene Symbol: SWT1
• Assay Reference Genome Location: Chr.1:185159576 on build GRCh38
• Cytoband: 1q25.3

Target Gene Details

• Entrez Gene ID: 54823
• Gene Name: SWT1, RNA endoribonuclease homolog
• Gene Aliases: C1orf26, HsSwt1
• Location: Chr.1:185157023-185291781 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
SWT1	NM_001105518.1			NP_001098988.1
	NM_017673.6			NP_060143.4
	XM_005245271.1			XP_005245328.1
	XM_005245273.1			XP_005245330.1
	XM_011509657.1			XP_011507959.1
	XM_017001527.1			XP_016857016.1
	XM_017001528.1			XP_016857017.1
	XM_017001529.1			XP_016857018.1
	XM_017001530.1			XP_016857019.1
	AK127980.1
	AK291443.1
	AK315802.1
	BC030781.2			AAH30781.1
	DB453411.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv548396	Chr.1:185068972 - 185182246 on Build GRCh38	Loss	TRMT1L SWT1 RNF2
nsv521613	Chr.1:185102699 - 185202737 on Build GRCh38	Loss	TRMT1L SWT1
esv3575349	Chr.1:185128640 - 185163037 on Build GRCh38	Gain	TRMT1L SWT1

More Information

Additional Information:

For this assay, SNP(s) [rs112528110] 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