Product Details

SNP ID: rs201998249
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:134199106 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CTTACAAAGAGTATTTTAGAGTATC[A/G]TCAAGTTCCATGATTGCAGCTTGGT
Phenotype: MIM: 176915
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: PPP2CA PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002715.2	1235	Silent Mutation	GAC,GAT	D279D	NP_002706.1