Assay Details
Target Gene Details
Entrez Gene ID: | 100128788 |
Gene Name: | SRRM2 antisense RNA 1 |
Gene Aliases: |
- |
Location: |
Chr.16:2737076-2752600 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SRRM2-AS1 | NR_027275.1 | |||
AK056063.1 | ||||
DB448439.2 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv2760067 | Chr.16:2486824 - 2820535 on Build GRCh38 | Gain+Loss | FLJ42627 PDPK1 PRSS33 SRRM2 PRSS27 MIR3178 CEMP1 TBC1D24 SRRM2-AS1 ERVK13-1 AMDHD2 TCEB2 PRSS41 KCTD5 LOC652276 ATP6V0C PRSS21 |
nsv471073 | Chr.16:2687070 - 2773569 on Build GRCh38 | Loss | SRRM2-AS1 TCEB2 KCTD5 SRRM2 PRSS27 |
nsv833123 | Chr.16:2561247 - 2764988 on Build GRCh38 | Gain+Loss | SRRM2-AS1 ERVK13-1 FLJ42627 PDPK1 KCTD5 SRRM2 LOC652276 PRSS27 |
More Information
Additional Information:
For this assay, SNP(s) [rs115989768] 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 |