Product Details

SNP ID
rs73999611
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.2:237087123 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTGTTTTGTTTTCATTTTTGGCCTT[C/T]TAGGCCCCTGGAGGAATTGCTACAC
Phenotype
MIM: 616011
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
COPS8 PubMed Links
Additional Information
For this assay, SNP(s) [rs138951874] are located under a primer 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.

Gene Details

Gene
COPS8
Gene Name
COP9 signalosome subunit 8
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_006710.4 Intron NP_006701.1
NM_198189.2 Intron NP_937832.1

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