Product Details

SNP ID

rs9427398

Assay Type

Functionally Tested

NCBI dbSNP Submissions

52

Location

Chr.1:161506415 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAGGACTCTGTGACTCTGACATGCC[A/G]GGGGGCTCGCAGCCCTGAGAGCGAC

Phenotype

MIM: 146790

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

FCGR2A PubMed Links

Additional Information

For this assay, SNP(s) [rs9427397] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

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	226	Missense Mutation	CAG,CGG	Q63R	NP_001129691.1
NM_021642.3	226	Missense Mutation	CAG,CGG	Q62R	NP_067674.2
XM_011509287.2	226	Missense Mutation	CAG,CGG	Q63R	XP_011507589.1
XM_011509290.2	226	Missense Mutation	CAG,CGG	Q63R	XP_011507592.1
XM_011509291.1	226	Missense Mutation	CAG,CGG	Q63R	XP_011507593.1
XM_017000663.1	226	Missense Mutation	CAG,CGG	Q62R	XP_016856152.1
XM_017000664.1	226	Missense Mutation	CAG,CGG	Q63R	XP_016856153.1
XM_017000665.1	226	Missense Mutation	CAG,CGG	Q63R	XP_016856154.1
XM_017000666.1	226	Missense Mutation	CAG,CGG	Q63R	XP_016856155.1
XM_017000667.1	226	Missense Mutation	CAG,CGG	Q63R	XP_016856156.1
XM_017000668.1	226	Missense Mutation	CAG,CGG	Q62R	XP_016856157.1

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