Product Details
- SNP ID
-
rs61740504
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.10:59793005 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GGGGACCGTGGGCTGCATGGGTGGC[A/G]GAGGTGGAGGCGGAGGTGGCTGGAC
- Phenotype
-
MIM: 601985
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
CCDC6
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs7899254] 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
- CCDC6
- Gene Name
- coiled-coil domain containing 6
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_005436.4 |
1569 |
Missense Mutation |
CCG,CTG |
P446L |
NP_005427.2 |
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