Product Details
- SNP ID
-
rs186169944
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.11:104887274 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AGATAATTTGGGAAATGAAGACAGA[A/G]CCATTTGTTTCATGTCTCCAAGAAA
- Phenotype
-
MIM: 608633
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
CASP12
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs142269030] 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
- CASP12
- Gene Name
- caspase 12 (gene/pseudogene)
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001191016.2 |
1105 |
Silent Mutation |
GGC,GGT |
G283G |
NP_001177945.2 |
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