Product Details

SNP ID
rs199808617
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.6:138092096 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGCATTGCCCAGAAGGTCATCTTC[A/G]TAGTTGGGGAGGCAGCAGAAGAAGA
Phenotype
MIM: 609301
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
PERP PubMed Links
Additional Information
For this assay, SNP(s) [rs648396] 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
PERP
Gene Name
PERP, TP53 apoptosis effector
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_022121.4 711 Silent Mutation TAC,TAT Y176Y NP_071404.2

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