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ATCCCAGATGACCCTTTGGTGCTCC[G/T]GACCCAGGGGAAGGTTTCATCTGTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
CES4A 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
|
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
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CES4A - carboxylesterase 4A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001190201.1 | 1317 | Missense Mutation | CGG,CTG | R,L 237 | NP_001177130.1 | |
NM_001190202.1 | 1317 | Missense Mutation | CGG,CTG | R,L 241 | NP_001177131.1 | |
NM_001318506.1 | 1317 | Missense Mutation | CGG,CTG | R,L 141 | NP_001305435.1 | |
NM_173815.6 | 1317 | Missense Mutation | CGG,CTG | R,L 335 | NP_776176.5 | |
XM_005255896.4 | 1317 | Missense Mutation | CGG,CTG | R,L 358 | XP_005255953.1 | |
XM_011523021.2 | 1317 | Missense Mutation | CGG,CTG | R,L 402 | XP_011521323.1 | |
XM_011523023.2 | 1317 | Missense Mutation | CGG,CTG | R,L 398 | XP_011521325.1 | |
XM_011523024.2 | 1317 | Missense Mutation | CGG,CTG | R,L 402 | XP_011521326.1 | |
XM_011523025.2 | 1317 | Missense Mutation | CGG,CTG | R,L 402 | XP_011521327.1 | |
XM_011523026.2 | 1317 | Missense Mutation | CGG,CTG | R,L 362 | XP_011521328.1 | |
XM_011523027.2 | 1317 | Missense Mutation | CGG,CTG | R,L 402 | XP_011521329.1 | |
XM_011523028.2 | 1317 | Missense Mutation | CGG,CTG | R,L 350 | XP_011521330.1 | |
XM_011523029.2 | 1317 | Missense Mutation | CGG,CTG | R,L 402 | XP_011521331.1 | |
XM_011523030.2 | 1317 | Missense Mutation | CGG,CTG | R,L 358 | XP_011521332.1 | |
XM_017023160.1 | 1317 | Missense Mutation | CGG,CTG | R,L 398 | XP_016878649.1 | |
XM_017023161.1 | 1317 | Missense Mutation | CGG,CTG | R,L 398 | XP_016878650.1 | |
XM_017023162.1 | 1317 | Missense Mutation | CGG,CTG | R,L 402 | XP_016878651.1 | |
XM_017023163.1 | 1317 | Missense Mutation | CGG,CTG | R,L 402 | XP_016878652.1 | |
XM_017023164.1 | 1317 | Missense Mutation | CGG,CTG | R,L 398 | XP_016878653.1 | |
XM_017023165.1 | 1317 | Missense Mutation | CGG,CTG | R,L 398 | XP_016878654.1 | |
XM_017023166.1 | 1317 | Missense Mutation | CGG,CTG | R,L 402 | XP_016878655.1 | |
XM_017023167.1 | 1317 | Missense Mutation | CGG,CTG | R,L 237 | XP_016878656.1 | |
XM_017023168.1 | 1317 | Missense Mutation | CGG,CTG | R,L 237 | XP_016878657.1 |