Product Details
- SNP ID
-
rs28429629
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.9:128063776 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- GGCTCTTGAGCGCTTGCGGCTTGAC[A/C]GACGTGTCTGCATGCTGGGCCATCA
- Phenotype
-
MIM: 610673
MIM: 608745
- Polymorphism
- A/C, Transversion Substitution
- Allele Nomenclature
-
- Literature Links
-
NAIF1
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs115369184] 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
- NAIF1
- Gene Name
- nuclear apoptosis inducing factor 1
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_197956.3 |
855 |
Silent Mutation |
|
|
NP_931045.1 |
- Gene
- SLC25A25
- Gene Name
- solute carrier family 25 member 25
There are no transcripts associated with this gene.
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