Product Details
- SNP ID
-
rs12082305
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
29
- Location
-
Chr.1:53227955 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- CAAAGGAAGACAATTACGCCCAACA[G/T]TTGCCAAAAGTGAGCCGTACCTAAT
- Phenotype
-
MIM: 602603
- Polymorphism
- G/T, Transversion Substitution
- Allele Nomenclature
-
- Literature Links
-
C1orf123
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs116135375] 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
- C1orf123
- Gene Name
- chromosome 1 open reading frame 123
There are no transcripts associated with this gene.
- Gene
- MAGOH
- Gene Name
- mago homolog, exon junction complex core component
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_002370.3 |
|
Intron |
|
|
NP_002361.1 |
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