Product Details

SNP ID
rs201295448
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.6:166307732 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCAGGACGGCCTCGGGGGTGAGATT[C/T]AGGCAGAAGCGCGCAGCGGAGTCTG
Phenotype
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
PRR18 PubMed Links
Additional Information
For this assay, SNP(s) [rs7757150] 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

Gene
PRR18
Gene Name
proline rich 18
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_175922.3 652 Silent Mutation CTA,CTG L137L NP_787118.2

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