Product Details
- SNP ID
-
rs149200159
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.2:231593050 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AAGGTCAGGTCCCACTCACAGCAGA[A/T]GTCTTGGCAGTGAGCAGCTCTGTCG
- Phenotype
-
- Polymorphism
- A/T, Transversion Substitution
- Allele Nomenclature
-
- Literature Links
-
C2orf57
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs16828251] 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
- C2orf57
- Gene Name
- chromosome 2 open reading frame 57
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_152614.2 |
187 |
Missense Mutation |
GAA,GAT |
E33D |
NP_689827.2 |
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