Assay Details
Target Gene Details
Entrez Gene ID: | 100129792 |
Gene Name: | coiled-coil domain containing 152 |
Gene Aliases: |
CH5400 |
Location: |
Chr.5:42756818-42802437 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
CCDC152 | NM_001134848.1 | NP_001128320.1 | ||
AK127368.1 | ||||
AK303469.1 | ||||
BC039102.1 | AAH39102.1 | |||
DB450032.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
dgv5637n100 | Chr.5:42609988 - 42844089 on Build GRCh38 | Gain | SEPP1 GHR CCDC152 |
nsv523033 | Chr.5:42751935 - 42919583 on Build GRCh38 | Gain | SEPP1 CCDC152 |
nsv597886 | Chr.5:42610307 - 42854306 on Build GRCh38 | Gain | SEPP1 GHR CCDC152 |
nsv597925 | Chr.5:42728729 - 43237086 on Build GRCh38 | Gain | SEPP1 FLJ32255 LOC100506639 ANXA2R NIM1K LOC648987 LOC153684 CCDC152 ZNF131 LOC100132356 |
More Information
Additional Information:
For this assay, SNP(s) [rs75455481] 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 |