Product Details
- SNP ID
-
rs146059128
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.12:45016291 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- ACACGGAGGAATGCTTCCATTCAGA[C/T]AGCCCCAGTAAGTACACCCTTGCTT
- Phenotype
-
- Polymorphism
- C/T, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
DBX2
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs1224442] 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
- DBX2
- Gene Name
- developing brain homeobox 2
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001004329.2 |
1187 |
Missense Mutation |
ATC,GTC |
I339V |
NP_001004329.2 |
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