Product Details

SNP ID
rs1504360
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.4:146639540 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AAATCACCCCACACCTCCAACCAAT[A/T]TTCCCCTCTCTCTCTCTTAAGTATT
Phenotype
MIM: 113725
Polymorphism
A/T, Transversion Substitution
Allele Nomenclature
Literature Links
POU4F2 PubMed Links
Additional Information
For this assay, SNP(s) [rs199989946] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene
POU4F2
Gene Name
POU class 4 homeobox 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_004575.2 Intron NP_004566.2

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