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CTGGAGATTGAAGGCAGTATCCAGA[A/C]ACTTCTTCAGTGACACCAGGTGAGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
OGDHL 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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OGDHL - oxoglutarate dehydrogenase-like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001143996.1 | 3011 | Missense Mutation | TGT,TTT | C,F 938 | NP_001137468.1 | |
NM_001143997.1 | 3011 | Missense Mutation | TGT,TTT | C,F 786 | NP_001137469.1 | |
NM_018245.2 | 3011 | Missense Mutation | TGT,TTT | C,F 995 | NP_060715.2 | |
XM_011539946.1 | 3011 | Missense Mutation | TGT,TTT | C,F 995 | XP_011538248.1 | |
XM_011539947.1 | 3011 | Missense Mutation | TGT,TTT | C,F 995 | XP_011538249.1 | |
XM_017016401.1 | 3011 | Missense Mutation | TGT,TTT | C,F 786 | XP_016871890.1 | |
XM_017016402.1 | 3011 | Missense Mutation | TGT,TTT | C,F 656 | XP_016871891.1 | |
XM_017016403.1 | 3011 | Missense Mutation | TGT,TTT | C,F 656 | XP_016871892.1 |