Product Details
- SNP ID
-
rs6969196
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.7:156950055 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- TGCAGAGGACGGCGGGCCCCGAACA[A/G]GGTCCCGGCCTGGGAGGCCGAAGCG
- Phenotype
-
MIM: 611269
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
NOM1
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs376182769] are located under a probe 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
- NOM1
- Gene Name
- nucleolar protein with MIF4G domain 1
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_138400.1 |
333 |
Silent Mutation |
CAA,CAG |
Q106Q |
NP_612409.1 |
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