Product Details
- SNP ID
-
rs150485964
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.5:146339606 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AGCCTGCTGGCACGCGCCGAAGCTC[C/T]GGCGGCGGTGGATATCGTCTCCCAC
- Phenotype
-
MIM: 602460
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
POU4F3
PubMed Links
Gene Details
- Gene
- POU4F3
- Gene Name
- POU class 4 homeobox 3
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_002700.2 |
268 |
Missense Mutation |
CCG,CTG |
P60L |
NP_002691.1 |
View Full Product Details