Product Details
- SNP ID
-
rs182879761
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.3:180616903 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AGTTGAAATGAATAAGCCTGCTTCT[C/T]TGATAACTTTTCTTTAACATTATTT
- Phenotype
-
MIM: 613798
- Polymorphism
- C/T, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
CCDC39
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs11914833] 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
- CCDC39
- Gene Name
- coiled-coil domain containing 39
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_181426.1 |
2444 |
Missense Mutation |
AAG,GAG |
K777E |
NP_852091.1 |
- Gene
- TTC14
- Gene Name
- tetratricopeptide repeat domain 14
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