Product Details
- SNP ID
-
rs199824066
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
2
- Location
-
Chr.1:27773336 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TCATACGGTCCCTTAGACATGTACC[A/G]GAACCCGGGGCCCTCGGGGCCCCAG
- Phenotype
-
MIM: 606892
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
STX12
PubMed Links
Gene Details
- Gene
- STX12
- Gene Name
- syntaxin 12
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_177424.2 |
154 |
Missense Mutation |
CAG,CGG |
Q10R |
NP_803173.1 |
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