Product Details
- SNP ID
-
rs2370706
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.2:186694326 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AACAGCAGCAGCAGCAGCAGCAACA[A/G]CAACAACAACAGCAAAAGCAGCTGG
- Phenotype
-
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
FAM171B
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs144403657] are located under a probe and SNP(s) [rs549897920] 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
- FAM171B
- Gene Name
- family with sequence similarity 171 member B
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_177454.3 |
265 |
Silent Mutation |
CAA,CAG |
Q51Q |
NP_803237.3 |
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