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CTCGGCAGCCTAGTGGATTGCCACC[A/G]TATGTGGACCCATGCTCCCCTGGCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613349 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
OAT 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
|
OAT - ornithine aminotransferase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000274.3 | Intron | NP_000265.1 | ||||
NM_001171814.1 | Intron | NP_001165285.1 | ||||
NM_001322965.1 | Intron | NP_001309894.1 | ||||
NM_001322966.1 | Intron | NP_001309895.1 | ||||
NM_001322967.1 | Intron | NP_001309896.1 | ||||
NM_001322968.1 | Intron | NP_001309897.1 | ||||
NM_001322969.1 | Intron | NP_001309898.1 | ||||
NM_001322970.1 | Intron | NP_001309899.1 | ||||
NM_001322971.1 | Intron | NP_001309900.1 | ||||
NM_001322974.1 | Intron | NP_001309903.1 | ||||
XM_017016279.1 | Intron | XP_016871768.1 |