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- SNP ID:
- rs1065658
- Gene
-
AKR7A3LOC100506730 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.1: 19284733 - 19284733 on Build GRCh38
- Polymorphism:
- G/A, Transition Substitution
- Context Sequence [VIC/FAM]:
AGGTATTCCCAAAGAAGCGGCCCAC[G/A]GGCTGTTTCCCATTCTTGTCCTCAT
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
30 submissions
|
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Phenotype: |
MIM: 608477
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Literature Links: |
AKR7A3 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
|
| AKR7A3 - aldo-keto reductase family 7 member A3 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_012067.2 | 468 | Silent Mutation | CCC,CCT | P,P 219 | NP_036199.2 | |
| XM_011541046.2 | 468 | Silent Mutation | CCC,CCT | P,P 219 | XP_011539348.1 | |
| XM_017000714.1 | 468 | Silent Mutation | CCC,CCT | P,P 148 | XP_016856203.1 | |
| LOC100506730 - uncharacterized LOC100506730 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
Back To TopMore Information
Additional Information:
For this assay, SNP(s) [rs1738023] 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.
Panther Classification:
Gene Ontology Categories:
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