Product Details

SNP ID: rs13152799
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.4:146639259 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: ACCTCGCCGGGCTCCTCGGCTCCCA[C/T]CGCGCCCTCGGCCAGCTCCCCCAGC
Phenotype: MIM: 113725
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: POU4F2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004575.2	367	Missense Mutation	ACC,ATC	T40I	NP_004566.2