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- SNP ID:
- rs140448519
- Gene
-
EEF1A1 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.6: 73516143 - 73516143 on Build GRCh38
- Polymorphism:
- A/T, Transversion Substitution
- Context Sequence [VIC/FAM]:
AGACTTGATACCTCAGAGCACTGGC[A/T]GATGGGAAGGCATTTTATCTAATTC
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 130590
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Literature Links: |
EEF1A1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
| EEF1A1 - eukaryotic translation elongation factor 1 alpha 1 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001402.5 | 3119 | UTR 3 | NP_001393.1 | |||
| XM_011535514.2 | 3119 | Intron | XP_011533816.1 | |||
Back To TopMore Information
Additional Information:
For this assay, SNP(s) [rs139487221] 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.
Panther Classification:
Gene Ontology Categories:
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