Product Details

SNP ID: rs181217345
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.8:30797643 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AAGAGATCTGTAAAATATTTCCAAA[C/T]GTTGGCATTCCCATACTTTCGCAGA
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	839	Missense Mutation	ATT,GTT	I142V	NP_001009552.1