Product Details
- SNP ID
-
rs4924454
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.15:40332573 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- TCAGTCCCATTGTGAGGGCTGAACC[C/G]GAGCTCTGCCTGCTTCCTACATCCT
- Phenotype
-
- Polymorphism
- C/G, Transversion Substitution
- Allele Nomenclature
-
- Literature Links
-
C15orf52
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs76448349] 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
- C15orf52
- Gene Name
- chromosome 15 open reading frame 52
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_207380.2 |
4206 |
UTR 3 |
|
|
NP_997263.2 |
- Gene
- INAFM2
- Gene Name
- InaF motif containing 2
There are no transcripts associated with this gene.
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