Product Details

SNP ID
rs3859072
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:67004118 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCATGAGCCCTGTGGTGGATGGTG[G/T]GGTGATCCCAGATGACCCTTTGGTG
Phenotype
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
CES4A PubMed Links

Gene Details

Gene
CES4A
Gene Name
carboxylesterase 4A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001190201.1 1287 Missense Mutation GGG,GTG G227V NP_001177130.1
NM_001190202.1 1287 Missense Mutation GGG,GTG G231V NP_001177131.1
NM_001318506.1 1287 Missense Mutation GGG,GTG G131V NP_001305435.1
NM_173815.6 1287 Missense Mutation GGG,GTG G325V NP_776176.5
XM_005255896.4 1287 Missense Mutation GGG,GTG G348V XP_005255953.1
XM_011523021.2 1287 Missense Mutation GGG,GTG G392V XP_011521323.1
XM_011523023.2 1287 Missense Mutation GGG,GTG G388V XP_011521325.1
XM_011523024.2 1287 Missense Mutation GGG,GTG G392V XP_011521326.1
XM_011523025.2 1287 Missense Mutation GGG,GTG G392V XP_011521327.1
XM_011523026.2 1287 Missense Mutation GGG,GTG G352V XP_011521328.1
XM_011523027.2 1287 Missense Mutation GGG,GTG G392V XP_011521329.1
XM_011523028.2 1287 Missense Mutation GGG,GTG G340V XP_011521330.1
XM_011523029.2 1287 Missense Mutation GGG,GTG G392V XP_011521331.1
XM_011523030.2 1287 Missense Mutation GGG,GTG G348V XP_011521332.1
XM_017023160.1 1287 Missense Mutation GGG,GTG G388V XP_016878649.1
XM_017023161.1 1287 Missense Mutation GGG,GTG G388V XP_016878650.1
XM_017023162.1 1287 Missense Mutation GGG,GTG G392V XP_016878651.1
XM_017023163.1 1287 Missense Mutation GGG,GTG G392V XP_016878652.1
XM_017023164.1 1287 Missense Mutation GGG,GTG G388V XP_016878653.1
XM_017023165.1 1287 Missense Mutation GGG,GTG G388V XP_016878654.1
XM_017023166.1 1287 Missense Mutation GGG,GTG G392V XP_016878655.1
XM_017023167.1 1287 Missense Mutation GGG,GTG G227V XP_016878656.1
XM_017023168.1 1287 Missense Mutation GGG,GTG G227V XP_016878657.1

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