Assay Details
Target Gene Details
Entrez Gene ID: | 196913 |
Gene Name: | long intergenic non-protein coding RNA 1599 |
Gene Aliases: |
C14orf183 |
Location: |
Chr.14:50007313-50105043 on Build GRCh38 |
Assay Gene Location: | Within Intron 6 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
LINC01599 | NR_131171.1 | |||
BQ027525.1 | ||||
BU927649.1 | ||||
DA856251.1 | ||||
T90102.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv28926 | Chr.14:49426970 - 50475809 on Build GRCh38 | Gain+Loss | POLE2 VCPKMT DNAAF2 MIR6076 LOC100288910 KLHDC1 LOC100506446 MAP4K5 NEMF ATP5S MIR4504 LRR1 RN7SL2 RN7SL1 LINC01588 KLHDC2 MGAT2 ARF6 SOS2 L2HGDH RPL36AL LINC01599 CDKL1 RPS29 |
More Information
Additional Information:
For this assay, SNP(s) [rs79691522] 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 |