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TGTTCGCTCCAACCCGGGGGCTCAG[A/G]CCCACCTCGATCCCGCCTTCCCGGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 152391 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ALOX12 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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ALOX12 - arachidonate 12-lipoxygenase, 12S type | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000697.2 | 1997 | Intron | NP_000688.2 | |||
XM_011523780.2 | 1997 | Silent Mutation | AGA,AGG | R,R 9 | XP_011522082.1 |
ALOX12-AS1 - ALOX12 antisense RNA 1 | ||||||
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There are no transcripts associated with this gene. |