Product Details

SNP ID: rs114227339
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:134204264 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GTCTGTTGCCTAGGGGGGAAAAAAT[C/T]TCCCCAAGATTTTTGGGTAAAGGTA
Phenotype: MIM: 176915
Polymorphism: C/T, 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		Intron			NP_002706.1