Product Details
- SNP ID
-
rs17199614
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.2:231593146 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- CCACCCCCAGGGCCATATCAACATC[C/T]GGAGACAAAGACAAGAGTGCAGTTG
- Phenotype
-
- Polymorphism
- C/T, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
C2orf57
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs74460533] 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 |
283 |
Silent Mutation |
TCC,TCT |
S65S |
NP_689827.2 |
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