Product Details

SNP ID: rs113782797
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.8:30794016 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GTCCAAATGTGTAGCCAGCACCACG[C/T]GGTGAAATACCCCATCCACCACGAT
Phenotype: MIM: 176916
Polymorphism: C/T, Transition 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	1054	Silent Mutation	CCA,CCG	P213P	NP_001009552.1