Assay Details
Target Gene Details
Entrez Gene ID: | 255082 |
Gene Name: | cancer susceptibility candidate 2 (non-protein coding) |
Gene Aliases: |
C10orf5 |
Location: |
Chr.10:118046821-118210153 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CASC2 | NR_026939.1 | |||
| NR_026940.1 | ||||
| NR_026941.1 | ||||
| AJ344228.1 | CAC83044.1 | |||
| AJ535620.1 | CAD59605.1 | |||
| AJ535621.1 | CAD59606.1 | |||
| AY226450.1 | AAP48615.1 | |||
| AY226451.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1047815 | Chr.10:118004235 - 118069532 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs73411833] 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: |
|

Genomic Map