Product Details

SNP ID
rs201218628
Assay Type
Functionally tested
NCBI dbSNP Submissions
1
Location
Chr.1:161506414 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAGGACTCTGTGACTCTGACATGC[CA/TG]GGGGGCTCGCAGCCCTGAGAGCGA
Phenotype
MIM: 146790
Polymorphism
CA/TG, Multiple nucleotide polymorphism
Allele Nomenclature
Literature Links
FCGR2A PubMed Links

Gene Details

Gene
FCGR2A
Gene Name
Fc fragment of IgG receptor IIa
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001136219.1 225 Silent Mutation CAA,CAG Q63Q NP_001129691.1
NM_021642.3 225 Silent Mutation CAA,CAG Q62Q NP_067674.2
XM_011509287.2 225 Silent Mutation CAA,CAG Q63Q XP_011507589.1
XM_011509290.2 225 Nonsense Mutation CAG,TGA Q63* XP_011507592.1
XM_011509291.1 225 Silent Mutation CAA,CAG Q63Q XP_011507593.1
XM_017000663.1 225 Silent Mutation CAA,CAG Q62Q XP_016856152.1
XM_017000664.1 225 Silent Mutation CAA,CAG Q63Q XP_016856153.1
XM_017000665.1 225 Silent Mutation CAA,CAG Q63Q XP_016856154.1
XM_017000666.1 225 Silent Mutation CAA,CAG Q63Q XP_016856155.1
XM_017000667.1 225 Silent Mutation CAA,CAG Q63Q XP_016856156.1
XM_017000668.1 225 Silent Mutation CAA,CAG Q62Q XP_016856157.1

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