Product Details

SNP ID
rs1059004
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.21:33028155 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACTAGAACTCATCCGACCCCCGACC[A/C]CCACCTCCGGGAAAAGATTCTAAAA
Phenotype
MIM: 606386
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
OLIG2 PubMed Links
Additional Information
For this assay, SNP(s) [rs6517136] 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
OLIG2
Gene Name
oligodendrocyte lineage transcription factor 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_005806.3 1681 UTR 3 NP_005797.1
XM_005260908.1 1681 UTR 3 XP_005260965.1

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