Product Details
- SNP ID
-
rs151233771
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.21:32582291 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CAGCTGCAGAGCTCTCAGCTTTTCT[C/T]GGAGCTCCATGTTCTGCTCCCTCAA
- Phenotype
-
MIM: 608365
- Polymorphism
- C/T, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
TCP10L
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs142055069] 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
- TCP10L
- Gene Name
- t-complex 10-like
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_144659.5 |
385 |
Missense Mutation |
CAA,CGA |
Q90R |
NP_653260.1 |
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