Product Details

SNP ID: rs17885558
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.7:95359938 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TTATCAGTTTACTTTTACAAAATAT[A/G]TAGACTTTTTTTTTTTTTTTTTACT
Phenotype: MIM: 602720
Polymorphism: A/G, Transition Substitution
Allele Nomenclature
Literature Links: PON3 PubMed Links
Additional Information: For this assay, SNP(s) [rs553882161] 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_000940.2	1125	UTR 3			NP_000931.1