Product Details

SNP ID: rs200382055
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.4:73869478 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: ACCCGCCTGCTGAGCCCCATGGCCC[G/T]CGCTGCTCTCTCCGCCGCCCCCAGC
Phenotype: MIM: 155730
Polymorphism: G/T, Transversion Substitution
Allele Nomenclature
Literature Links: CXCL1 PubMed Links
Additional Information: For this assay, SNP(s) [rs11547681] 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

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001511.3	87	Missense Mutation	CGC,CTC	R3L	NP_001502.1