Product Details

SNP ID: rs149781521
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:134201989 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TGATCTGTCTGCTCTCATGATTCCC[G/T]CGAAGAATGGTGATGCGTTCACGGT
Phenotype: MIM: 176915
Polymorphism: G/T, Transversion 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	743	Silent Mutation	CGA,CGC	R115R	NP_002706.1