Product Details
- SNP ID
-
rs200220379
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.4:73998227 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TTACACCACTTCCACCTTGGAGCAC[C/T]GTGGGCCTATGGCGAACACTTGCAG
- Phenotype
-
MIM: 600324
- Polymorphism
- C/T, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
CXCL5
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs425535] 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
- CXCL5
- Gene Name
- C-X-C motif chemokine ligand 5
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_002994.4 |
369 |
Missense Mutation |
CAG,CGG |
Q74R |
NP_002985.1 |
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