Product Details
- SNP ID
-
rs199711565
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.11:122977657 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CTCCCCAGCCTGGCGGCTCAGAGCA[C/G]GTGCGGCCCTGAGCCCAGCTCCCCC
- Phenotype
-
MIM: 611074
- Polymorphism
- C/G, Transversion Substitution
- Allele Nomenclature
-
- Literature Links
-
BSX
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs61737277] 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
- BSX
- Gene Name
- brain specific homeobox
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001098169.1 |
694 |
Missense Mutation |
CTG,GTG |
L232V |
NP_001091639.1 |
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