Product Details

SNP ID: rs139883264
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.4:146640037 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TGAATACCATCCCGTGCACGTCGGC[C/T]GCCTCTTCTTCATCGGTGCCCATCT
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	707	Silent Mutation	GCC,GCT	A153A	NP_004566.2