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TTCAGAGGACTGCCTGGTCCTCAAC[A/G]TCTATAGCCCAGCTGAGGTCCCCGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605279 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CES3 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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CES3 - carboxylesterase 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001185176.1 | 464 | Intron | NP_001172105.1 | |||
NM_001185177.1 | 464 | Missense Mutation | ATC,GTC | I,V 129 | NP_001172106.1 | |
NM_024922.5 | 464 | Missense Mutation | ATC,GTC | I,V 129 | NP_079198.2 | |
XM_011522975.2 | 464 | Intron | XP_011521277.1 | |||
XM_011522976.2 | 464 | Missense Mutation | ATC,GTC | I,V 129 | XP_011521278.1 |