Product Details

SNP ID: rs10089206
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.8:30789727 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TGATGAGAGGTTGTGTTTAAGCCTC[A/C]CATACTAGTGATGGTTACACCATTT
Phenotype: MIM: 176916
Polymorphism: A/C, Transversion Substitution
Allele Nomenclature
Literature Links: PPP2CB PubMed Links
Additional Information: For this assay, SNP(s) [rs149223680] 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_001009552.1		Intron			NP_001009552.1