Product Details

SNP ID: rs7705270
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:134204308 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: AAAGGTAAAGTCAAACAATTTATTT[A/C]AAGGGAAAGGCGGAAGCCTGCCACC
Phenotype: MIM: 176915
Polymorphism: A/C, 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		Intron			NP_002706.1