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GGGGAGTCTTGTCCATGTGAAGGGC[A/G]CCAATGCCGGGGTCCAAACCTTCCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605278 MIM: 614778 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CES2 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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CES2 - carboxylesterase 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003869.5 | 1343 | Missense Mutation | ACC,GCC | T,A 115 | NP_003860.2 | |
NM_198061.2 | 1343 | Missense Mutation | ACC,GCC | T,A 115 | NP_932327.1 | |
XM_011523421.2 | 1343 | UTR 5 | XP_011521723.1 | |||
XM_017023818.1 | 1343 | UTR 5 | XP_016879307.1 |
FAM96B - family with sequence similarity 96 member B | ||||||
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There are no transcripts associated with this gene. |