Assay Details
Target Gene Details
Entrez Gene ID: | 51079 |
Gene Name: | NADH:ubiquinone oxidoreductase subunit A13 |
Gene Aliases: |
B16.6, CDA016, CGI-39, GRIM-19, GRIM19 |
Location: |
Chr.19:19516210-19528204 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
NDUFA13 | NM_015965.6 | NP_057049.5 | ||
AF261134.1 | AAG44670.1 | |||
AF286697.1 | AAG28167.1 | |||
AK293859.1 | ||||
BC000589.2 | AAH00589.2 | |||
BC009189.2 | AAH09189.1 | |||
BG705222.1 | ||||
BM839920.1 | ||||
BP230223.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv509723 | Chr.19:19517547 - 19595561 on Build GRCh38 | Insertion | NDUFA13 PBX4 CILP2 YJEFN3 |
nsv952426 | Chr.19:19525792 - 19601091 on Build GRCh38 | Deletion | NDUFA13 PBX4 CILP2 YJEFN3 |
More Information
Additional Information:
For this assay, SNP(s) [rs73002997] 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 |