Product Details
- SNP ID
-
rs1782996
- Assay Type
- Validated
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.21:34082467 on Build GRCh38
- Set Membership
-
HapMap
Validated
- Context Sequence [VIC/FAM]
- TATTAGTACTATTTGGTTTGTACCC[A/G]TTGTATTAACCTCTTAGGTGTTTGA
- Phenotype
-
MIM: 611973
MIM: 600444
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
MRPS6
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs73899950] 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
- MRPS6
- Gene Name
- mitochondrial ribosomal protein S6
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_032476.3 |
|
Intron |
|
|
NP_115865.1 |
- Gene
- SLC5A3
- Gene Name
- solute carrier family 5 member 3
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_006933.6 |
|
Intron |
|
|
NP_008864.4 |
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