Product Details
- SNP ID
-
rs183924846
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.16:69742548 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GCAGCTGAGGGAAGCGCTGATCCTC[A/G]GTGAGATGGGGGTTGATGGCGTATT
- Phenotype
-
MIM: 613586
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
NOB1
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs1075935] 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
- NOB1
- Gene Name
- NIN1/PSMD8 binding protein 1 homolog
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_014062.2 |
|
Intron |
|
|
NP_054781.1 |
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