Product Details
- SNP ID
-
rs201781902
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.6:98834883 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TCCGGCTCCGAGAGTCATGGCGACC[A/G]CAGCGTCTAACCACTACAGCCTGCT
- Phenotype
-
MIM: 600494
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
POU3F2
PubMed Links
Gene Details
- Gene
- POU3F2
- Gene Name
- POU class 3 homeobox 2
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_005604.3 |
180 |
Missense Mutation |
ACA,GCA |
T4A |
NP_005595.2 |
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