Assay Details
Target Gene Details
Entrez Gene ID: | 112950 |
Gene Name: | mediator complex subunit 8 |
Gene Aliases: |
ARC32 |
Location: |
Chr.1:43383908-43389812 on Build GRCh38 |
Assay Gene Location: | Within Exon 7 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
MED8 | NM_001001653.2 | 7 | 1637 | NP_001001653.1 |
NM_052877.4 | 8 | 1101 | NP_443109.2 | |
NM_201542.4 | 7 | 1594 | NP_963836.2 | |
BC010543.1 | 7 | 1042 | ||
BF196855.1 | 1 | 399 | ||
CB161514.1 | 1 | 494 | ||
CB162354.1 | 1 | 494 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv546128 | Chr.1:43301467 - 43451738 on Build GRCh38 | Loss | MED8 MIR6735 MPL HYI CDC20 ELOVL1 MIR6734 TIE1 SZT2 |
More Information
Additional Information:
For this assay, SNP(s) [rs118153648] 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 Exonic DGV Variation |