Product Details
- SNP ID
-
rs17766628
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.9:102997162 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- TATAAATCCTGGCACCACTCACATC[A/G]TAGTCTAGAAAACTTTTTGTTGGAA
- Phenotype
-
MIM: 604035
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
CYLC2
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs117780412] are located under a probe and SNP(s) [rs80042499] 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
- CYLC2
- Gene Name
- cylicin 2
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001340.4 |
|
Intron |
|
|
NP_001331.1 |
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