Product Details

SNP ID
rs28734117
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.15:48181837 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTATGGTATAATTTTTAAGTCAATT[C/T]GCTTCACTATATAAATTGCTGGATT
Phenotype
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
CTXN2 PubMed Links
Additional Information
For this assay, SNP(s) [rs75593588] 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
CTXN2
Gene Name
cortexin 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001145668.1 Intron NP_001139140.1
XM_005254378.3 Intron XP_005254435.1
XM_006720504.2 Intron XP_006720567.1
XM_011521553.1 Intron XP_011519855.1
XM_017022178.1 Intron XP_016877667.1
Gene
MYEF2
Gene Name
myelin expression factor 2
There are no transcripts associated with this gene.

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