Product Details

SNP ID: rs2411
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.20:46541166 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CATGATGCAAGGTCTCCATCTAACA[A/G]GTAGAGCAGTTGGTGCAGATGAGAT
Phenotype
Polymorphism: A/G, Transition Substitution
Allele Nomenclature
Literature Links: OCSTAMP PubMed Links
Additional Information: For this assay, SNP(s) [rs74370887] 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

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_080721.2	1545	UTR 3			NP_542452.1
XM_011528532.2	1545	UTR 3			XP_011526834.1