Product Details

SNP ID
rs140444624
Assay Type
Functionally Tested
NCBI dbSNP Submissions
16
Location
Chr.1:182600492 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGCAGGTTCATCCTCGTCAGCTCGT[A/G]GGTCTCATGGTCAATGTTGACCTGC
Phenotype
MIM: 602514
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
RGS16 PubMed Links
Additional Information
For this assay, SNP(s) [rs1144566] 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
RGS16
Gene Name
regulator of G-protein signaling 16
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_002928.3 563 Missense Mutation NP_002919.3

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