Product Details

SNP ID: rs13268487
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.8:30789023 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TCTACTTCCCCCATAGTGTGCAGCC[C/T]CTGTGGCCCTGCTCGGATGTTTTTA
Phenotype: MIM: 176916
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: PPP2CB PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001009552.1		Intron			NP_001009552.1