Product Details
- SNP ID
-
rs9904079
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.17:67046578 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- TGTGGCCATGTGCTTGCAGGGTATC[A/G]CATAGCCCGGATGCCCATGCCCCTT
- Phenotype
-
MIM: 114209
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
CACNG1
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs77717096] 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
- CACNG1
- Gene Name
- calcium voltage-gated channel auxiliary subunit gamma 1
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_000727.3 |
|
Intron |
|
|
NP_000718.1 |
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