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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