Hs05137445_cn

• Gene Symbol: LRRC27
• Assay Reference Genome Location: Chr.10:132338438 on build GRCh38
• Cytoband: 10q26.3

Target Gene Details

• Entrez Gene ID: 80313
• Gene Name: leucine rich repeat containing 27
• Gene Aliases: -
• Location: Chr.10:132330063-132381506 on Build GRCh38
• Assay Gene Location: Within Intron 6

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
LRRC27	NM_001143757.1			NP_001137229.1
	NM_001143758.1			NP_001137230.1
	NM_001143759.1			NP_001137231.1
	NM_001309474.1			NP_001296403.1
	NM_030626.2			NP_085129.1
	XM_006717983.2			XP_006718046.1
	XM_006717984.2			XP_006718047.1
	XM_011540208.1			XP_011538510.1
	XM_011540209.1			XP_011538511.1
	XM_011540210.2			XP_011538512.1
	XM_017016690.1			XP_016872179.1
	XM_017016691.1			XP_016872180.1
	XM_017016692.1			XP_016872181.1
	XM_017016693.1			XP_016872182.1
	XM_017016694.1			XP_016872183.1
	AB051461.1
	AK093250.1			BAC04108.1
	AK097418.1
	AK098652.1			BAC05366.1
	AK295953.1
	AK301422.1
	BC050097.1			AAH50097.1
	DA658738.1
	DC352688.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv1054569	Chr.10:132009350 - 132351508 on Build GRCh38	Gain	LRRC27 DPYSL4 STK32C JAKMIP3
esv3624988	Chr.10:132338306 - 132366249 on Build GRCh38	Gain	LRRC27
nsv1051555	Chr.10:132295188 - 132415461 on Build GRCh38	Gain	PWWP2B LRRC27 STK32C
esv3624986	Chr.10:132322882 - 132551350 on Build GRCh38	Gain	PWWP2B LRRC27 LOC105378568 C10orf91 STK32C INPP5A LOC107984282
esv2761642	Chr.10:132048518 - 132365985 on Build GRCh38	Gain	LRRC27 DPYSL4 STK32C JAKMIP3
nsv1054934	Chr.10:130334322 - 133158679 on Build GRCh38	Gain	PWWP2B LOC105378568 LINC01164 LINC01167 MIR378C C10orf91 CFAP46 NKX6-2 LINC01166 JAKMIP3 ADGRA1-AS1 INPP5A LRRC27 DPYSL4 STK32C PPP2R2D TCERG1L-AS1 BNIP3 ADGRA1 TCERG1L LOC107984282 LINC01168
nsv1052405	Chr.10:132336481 - 132390781 on Build GRCh38	Gain	LRRC27

More Information

Additional Information:

For this assay, SNP(s) [rs114174684,rs145764141] 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