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- SNP ID:
- rs9898751
- Gene
-
ALOX15BLOC105371518 - Gene Name
- Set Membership:
- > HapMap
- Chromosome Location:
- Chr.17: 8047634 - 8047634 on Build GRCh38
- Polymorphism:
- A/C, Transversion substitution
- Context Sequence [VIC/FAM]:
TCACCATGGTGATATTCACCTGCTC[A/C]GCCAAGCATGCGGCTGTCAGTGCAG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603697
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Literature Links: |
ALOX15B PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | ||||||
|---|---|---|---|---|---|---|---|---|
Global
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Caucasian - Not Available | CEPH (CEU)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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| ALOX15B - arachidonate 15-lipoxygenase, type B | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001039130.1 | 1679 | Silent Mutation | TCA,TCC | S,S 521 | NP_001034219.1 | |
| NM_001039131.1 | 1679 | Silent Mutation | TCA,TCC | S,S 476 | NP_001034220.1 | |
| NM_001141.2 | 1679 | Silent Mutation | TCA,TCC | S,S 550 | NP_001132.2 | |
| LOC105371518 - uncharacterized LOC105371518 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
Back To TopMore Information
Set Membership: |
HapMap
|
Panther Classification:
Gene Ontology Categories:
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