Assay Details
Target Gene Details
Entrez Gene ID: | 284498 |
Gene Name: | chromosome 1 open reading frame 167 |
Gene Aliases: |
- |
Location: |
Chr.1:11762188-11789585 on Build GRCh38 |
Assay Gene Location: | Within Intron 20 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
C1orf167 | NM_001010881.1 | NP_001010881.1 | ||
XM_011541269.2 | XP_011539571.2 | |||
XM_011541271.2 | XP_011539573.2 | |||
XM_011541272.2 | XP_011539574.1 | |||
XM_011541274.2 | XP_011539576.2 | |||
XM_011541275.2 | XP_011539577.2 | |||
XM_011541276.2 | XP_011539578.1 | |||
XM_011541277.2 | XP_011539579.1 | |||
XM_011541278.2 | XP_011539580.1 | |||
XM_011541280.2 | XP_011539582.2 | |||
XM_011541281.2 | XP_011539583.2 | |||
XM_017001062.1 | XP_016856551.1 | |||
XM_017001063.1 | XP_016856552.1 | |||
XM_017001064.1 | XP_016856553.1 | |||
AL833926.1 | CAD38782.1 | |||
AL834308.1 | CAD38978.2 | |||
BC031692.1 |
More Information
Additional Information:
For this assay, SNP(s) [rs75559897] 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 non-DGV Variation |