Product Details
- SNP ID
-
rs3917436
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
35
- Location
-
Chr.1:169725478 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- AGCTTAGAAAAATTCCCAGAATATA[G/A]TAAGTGCAATGTAAGGGTCAGCTAT
- Phenotype
-
MIM: 131210
- Polymorphism
- G/A, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
SELE
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs3917434] 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
- SELE
- Gene Name
- selectin E
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_000450.2 |
|
Intron |
|
|
NP_000441.2 |
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