Assay Details
Target Gene Details
Entrez Gene ID: | 10930 |
Gene Name: | apolipoprotein B mRNA editing enzyme catalytic subunit 2 |
Gene Aliases: |
ARCD1, ARP1 |
Location: |
Chr.6:41053201-41064891 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
APOBEC2 | NM_006789.3 | NP_006780.1 | ||
AF161698.1 | AAD45360.1 | |||
AK223461.1 | BAD97181.1 | |||
AK300689.1 | ||||
AK308197.1 | ||||
AK310006.1 | ||||
AK313288.1 | ||||
BC047767.2 | AAH47767.1 | |||
BC069688.1 | AAH69688.1 | |||
BC069764.1 | AAH69764.1 | |||
BI438931.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv526577 | Chr.6:41037763 - 41061603 on Build GRCh38 | Loss | APOBEC2 UNC5CL TSPO2 |
More Information
Additional Information:
For this assay, SNP(s) [rs74853194] 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 |