Product Details

SNP ID
rs140090973
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.2:233034192 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATGAACCCATGCCCCTTGTATGACG[C/T]GCAGACGGGGACCCTCTTCCTCTTC
Phenotype
MIM: 605528
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
NEU2 PubMed Links
Additional Information
For this assay, SNP(s) [rs2233388] 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
NEU2
Gene Name
neuraminidase 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_005383.2 278 Missense Mutation GCG,GTG A93V NP_005374.2

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