Product Details

SNP ID: rs1519551
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.4:141649319 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TATTTTCACCCATAGTCCCAAGTAC[A/G]TTAACATATGTAGCATTCTCAAACT
Phenotype: MIM: 600554
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: IL15 PubMed Links
Additional Information: For this assay, SNP(s) [rs72712403] 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_000585.4		Intron			NP_000576.1
NM_172175.2		Intron			NP_751915.1