Product Details
- SNP ID
-
rs828909
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.2:216110582 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- GAAATGAAGAGTTGCTATGCTACCC[A/G]GTTTCTCTTTCTCAGTTTTCTTACT
- Phenotype
-
MIM: 194364
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
TMEM169
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs6746833] 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
- TMEM169
- Gene Name
- transmembrane protein 169
There are no transcripts associated with this gene.
- Gene
- XRCC5
- Gene Name
- X-ray repair cross complementing 5
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_021141.3 |
|
Intron |
|
|
NP_066964.1 |
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