Assay Details
Target Gene Details
Entrez Gene ID: | 149499 |
Gene Name: | leucine rich repeat containing 71 |
Gene Aliases: |
C1orf92 |
Location: |
Chr.1:156920608-156941208 on Build GRCh38 |
Assay Gene Location: | Within Intron 17 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
LRRC71 | XM_017000459.1 | XP_016855948.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv3890682 | Chr.1:156899922 - 156951428 on Build GRCh38 | Loss | ARHGEF11 MIR765 LRRC71 PEAR1 |
nsv831659 | Chr.1:156771159 - 156980204 on Build GRCh38 | Loss | ARHGEF11 NTRK1 MIR765 LRRC71 PRCC INSRR PEAR1 SH2D2A |
More Information
Additional Information:
For this assay, SNP(s) [rs149349489] 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 |