Assay Details
Target Gene Details
Entrez Gene ID: | 283673 |
Gene Name: | Ewing sarcoma associated transcript 1 |
Gene Aliases: |
LINC00277, NCRNA00277, TMEM84 |
Location: |
Chr.15:69080850-69095824 on Build GRCh38 |
Assay Gene Location: | Within Exon 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| EWSAT1 | NR_026949.1 | 3 | 773 | |
| AK091087.1 | 3 | 761 | BAC03580.1 | |
| AK097560.1 | 4 | 602 | ||
| AK292174.1 | 3 | 326 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1050604 | Chr.15:69065909 - 69107327 on Build GRCh38 | Gain |
|
| nsv569808 | Chr.15:69035886 - 69100053 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs75206632] 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: |
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Genomic Map