Assay Details
Target Gene Details
Entrez Gene ID: | 6129 |
Gene Name: | ribosomal protein L7 |
Gene Aliases: |
L7, humL7-1 |
Location: |
Chr.8:73290639-73294494 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
RPL7 | XM_006716463.2 | XP_006716526.1 | ||
AK291119.1 | ||||
AK313365.1 | ||||
X52967.1 | CAA37139.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv971665 | Chr.8:73291015 - 73293598 on Build GRCh38 | Duplication | RPL7 |
esv2737154 | Chr.8:71825978 - 73469084 on Build GRCh38 | Deletion | MSC RPL7 LOC101926908 KCNB2 MSC-AS1 RDH10 STAU2-AS1 C8orf89 RDH10-AS1 LOC392232 SBSPON STAU2 TERF1 TRPA1 |
More Information
Additional Information:
For this assay, SNP(s) [rs140937357] 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 |