Product Details

SNP ID
rs141959939
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.11:8984088 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAATCTTACCTTCAGAGATCGGAGA[A/G]TCTGTAGACCAAGGGACAAGTTTTT
Phenotype
MIM: 613125
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
NRIP3 PubMed Links
Additional Information
For this assay, SNP(s) [rs546646196] 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
NRIP3
Gene Name
nuclear receptor interacting protein 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_020645.2 713 Missense Mutation ACT,ATT T200I NP_065696.1
Gene
TMEM9B-AS1
Gene Name
TMEM9B antisense RNA 1
There are no transcripts associated with this gene.

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