Product Details
- SNP ID
-
rs857798
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
34
- Location
-
Chr.1:158835434 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- TGTTAGCGTATAAAAACACAACTGA[C/T]TTGTATGTGTTGCCTTTGATTCCTG
- Phenotype
-
MIM: 159553
- Polymorphism
- C/T, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
MNDA
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs79470892] 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
- MNDA
- Gene Name
- myeloid cell nuclear differentiation antigen
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_002432.1 |
|
Intron |
|
|
NP_002423.1 |
- Gene
- OR6N1
- Gene Name
- olfactory receptor family 6 subfamily N member 1
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