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- SNP ID:
- rs12868587
- Gene
-
CCNA1 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.13: 36435070 - 36435070 on Build GRCh38
- Polymorphism:
- A/G, Transition Substitution
- Context Sequence [VIC/FAM]:
TTGACTTTGTAAAATCACCTTGACC[A/G]GTCCCTTTTTCAGCTAGAAATGGTG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 604036
|
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Literature Links: |
CCNA1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
| CCNA1 - cyclin A1 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001111045.1 | Intron | NP_001104515.1 | ||||
| NM_001111046.1 | Intron | NP_001104516.1 | ||||
| NM_001111047.1 | Intron | NP_001104517.1 | ||||
| NM_003914.3 | Intron | NP_003905.1 | ||||
| XM_011535294.2 | Intron | XP_011533596.1 | ||||
| XM_011535295.2 | Intron | XP_011533597.1 | ||||
| XM_011535296.2 | Intron | XP_011533598.1 | ||||
Back To TopMore Information
Additional Information:
For this assay, SNP(s) [rs76163674] 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.
Panther Classification:
Gene Ontology Categories:
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