Hs06344151_cn

• Gene Symbol: PRH1-PRR4
• Assay Reference Genome Location: Chr.12:10877688 on build GRCh38
• Cytoband: 12p13.2

Target Gene Details

• Entrez Gene ID: 100533464
• Gene Name: PRH1-PRR4 readthrough
• Gene Aliases: PRH1
• Location: Chr.12:10845849-11171625 on Build GRCh38
• Assay Gene Location: Within Intron 7

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
PRH1-PRR4	NR_037918.2
	AB593030.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv3628543	Chr.12:10720386 - 10881212 on Build GRCh38	Gain	LOC101928162 TAS2R10 TAS2R8 YBX3 PRH1 PRH1-PRR4 PRR4 TAS2R7 TAS2R9
esv2759879	Chr.12:10817021 - 11561987 on Build GRCh38	Loss	TAS2R10 PRH1 TAS2R30 TAS2R14 PRB4 PRB2 TAS2R42 TAS2R46 TAS2R50 PRR4 PRH2 PRB1 TAS2R19 TAS2R20 TAS2R31 PRB3 SMIM10L1 TAS2R13 PRH1-TAS2R14 TAS2R43 PRH1-PRR4 LINC01252

More Information

Additional Information:

For this assay, SNP(s) [rs77582458] 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