Product Details
- SNP ID
-
rs143938073
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.4:146640025 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CCTACCACACTATGAATACCATCCC[A/G]TGCACGTCGGCCGCCTCTTCTTCAT
- Phenotype
-
MIM: 113725
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
POU4F2
PubMed Links
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 |
695 |
Silent Mutation |
CCA,CCG |
P149P |
NP_004566.2 |
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