Product Details
- SNP ID
-
rs76334242
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.14:69572727 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GTCGCCGAGGCTGAAGCTGCGGCCG[C/G]TGATCGGAACCAGGGTCAGGGCAGA
- Phenotype
-
- Polymorphism
- C/G, Transversion Substitution
- Allele Nomenclature
-
- Literature Links
-
CCDC177
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs7147881] 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
- CCDC177
- Gene Name
- coiled-coil domain containing 177
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001271507.1 |
1266 |
Missense Mutation |
ACC,AGC |
T299S |
NP_001258436.1 |
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