Assay Details
Target Gene Details
Entrez Gene ID: | 84515 |
Gene Name: | minichromosome maintenance 8 homologous recombination repair factor |
Gene Aliases: |
C20orf154, POF10, dJ967N21.5 |
Location: |
Chr.20:5950652-6000941 on Build GRCh38 |
Assay Gene Location: | Within Exon 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
MCM8 | NM_001281520.1 | 1 | 223 | NP_001268449.1 |
NM_001281521.1 | 1 | 223 | NP_001268450.1 | |
NM_001281522.1 | 1 | 223 | NP_001268451.1 | |
NM_032485.5 | 1 | 223 | NP_115874.3 | |
NM_182802.2 | 1 | 223 | NP_877954.1 | |
XM_011529387.2 | 1 | 186 | XP_011527689.1 | |
XM_017028105.1 | 1 | 198 | XP_016883594.1 | |
XM_017028106.1 | 1 | 185 | XP_016883595.1 | |
AJ439063.1 | 1 | 223 | CAD27750.1 | |
AK297806.1 | 1 | 156 | ||
BC101054.1 | AAI01055.1 | |||
BC101055.1 | AAI01056.1 | |||
BC101056.1 | AAI01057.1 | |||
BC101057.1 | AAI01058.1 |
More Information
Additional Information:
For this assay, SNP(s) [rs117380724,rs191935419] 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 non-DGV Variation |