Product Details

SNP ID
hCV26674349
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.2:108728222 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAGAGAGTGGTACCACAGGGTTTCC[A/G]AGATTTCCAAGGCTGATGAAAATTC
Phenotype
MIM: 601181
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
RANBP2 PubMed Links
Additional Information
For this assay, SNP(s) [rs116265631,rs185463867] 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
RANBP2
Gene Name
RAN binding protein 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_006267.4 Intron NP_006258.3

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