Product Details

SNP ID: rs61744399
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.16:67003151 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CGCGTTATTCAGACTTTTCATCACT[A/C]GTAACCCACTGAAAGTGGCCAAGGT
Phenotype
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: CES4A PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001190201.1	1085	Missense Mutation	AGT,CGT	S160R	NP_001177130.1
NM_001190202.1	1085	Missense Mutation	AGT,CGT	S164R	NP_001177131.1
NM_001318506.1	1085	Missense Mutation	AGT,CGT	S64R	NP_001305435.1
NM_173815.6	1085	Missense Mutation	AGT,CGT	S258R	NP_776176.5
XM_005255896.4	1085	Missense Mutation	AGT,CGT	S281R	XP_005255953.1
XM_011523021.2	1085	Missense Mutation	AGT,CGT	S325R	XP_011521323.1
XM_011523023.2	1085	Missense Mutation	AGT,CGT	S321R	XP_011521325.1
XM_011523024.2	1085	Missense Mutation	AGT,CGT	S325R	XP_011521326.1
XM_011523025.2	1085	Missense Mutation	AGT,CGT	S325R	XP_011521327.1
XM_011523026.2	1085	Missense Mutation	AGT,CGT	S285R	XP_011521328.1
XM_011523027.2	1085	Missense Mutation	AGT,CGT	S325R	XP_011521329.1
XM_011523028.2	1085	Missense Mutation	AGT,CGT	S273R	XP_011521330.1
XM_011523029.2	1085	Missense Mutation	AGT,CGT	S325R	XP_011521331.1
XM_011523030.2	1085	Missense Mutation	AGT,CGT	S281R	XP_011521332.1
XM_017023160.1	1085	Missense Mutation	AGT,CGT	S321R	XP_016878649.1
XM_017023161.1	1085	Missense Mutation	AGT,CGT	S321R	XP_016878650.1
XM_017023162.1	1085	Missense Mutation	AGT,CGT	S325R	XP_016878651.1
XM_017023163.1	1085	Missense Mutation	AGT,CGT	S325R	XP_016878652.1
XM_017023164.1	1085	Missense Mutation	AGT,CGT	S321R	XP_016878653.1
XM_017023165.1	1085	Missense Mutation	AGT,CGT	S321R	XP_016878654.1
XM_017023166.1	1085	Missense Mutation	AGT,CGT	S325R	XP_016878655.1
XM_017023167.1	1085	Missense Mutation	AGT,CGT	S160R	XP_016878656.1
XM_017023168.1	1085	Missense Mutation	AGT,CGT	S160R	XP_016878657.1