Product Details
- SNP ID
-
rs184591480
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.4:146639264 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GCCGGGCTCCTCGGCTCCCATCGCG[C/T]CCTCGGCCAGCTCCCCCAGCAGCTC
- Phenotype
-
MIM: 113725
- Polymorphism
- C/T, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
POU4F2
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs13152799] 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 |
372 |
Missense Mutation |
CCC,TCC |
P42S |
NP_004566.2 |
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