Product Details

SNP ID: rs10109293
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.8:30793690 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: ATCTGAATGAAGCATACAGGGAATT[A/T]TGGGGTACTATTTTTGTAACTTTTT
Phenotype: MIM: 176916
Polymorphism: A/T, Transversion 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