Product Details
- SNP ID
-
rs199561534
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.16:75204245 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CAGCGGGCGTGGTGGTAGAGCAGGT[A/G]CGGCTGCCCCAGGACACAATGCCCA
- Phenotype
-
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
CTRB2
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs4737] are located under a primer 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
- CTRB2
- Gene Name
- chymotrypsinogen B2
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001025200.3 |
741 |
Silent Mutation |
CGC,CGT |
R236R |
NP_001020371.3 |
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