Product Details

SNP ID

rs201099382

Assay Type

Functionally Tested

NCBI dbSNP Submissions

3

Location

Chr.1:161506420 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCTGTGACTCTGACATGCCAGGGG[G/T]CTCGCAGCCCTGAGAGCGACTCCAT

Phenotype

MIM: 146790

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

FCGR2A PubMed Links

Additional Information

For this assay, SNP(s) [rs9427397,rs9427398] 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	231	Missense Mutation	GCT,TCT	A65S	NP_001129691.1
NM_021642.3	231	Missense Mutation	GCT,TCT	A64S	NP_067674.2
XM_011509287.2	231	Missense Mutation	GCT,TCT	A65S	XP_011507589.1
XM_011509290.2	231	Missense Mutation	GCT,TCT	A65S	XP_011507592.1
XM_011509291.1	231	Missense Mutation	GCT,TCT	A65S	XP_011507593.1
XM_017000663.1	231	Missense Mutation	GCT,TCT	A64S	XP_016856152.1
XM_017000664.1	231	Missense Mutation	GCT,TCT	A65S	XP_016856153.1
XM_017000665.1	231	Missense Mutation	GCT,TCT	A65S	XP_016856154.1
XM_017000666.1	231	Missense Mutation	GCT,TCT	A65S	XP_016856155.1
XM_017000667.1	231	Missense Mutation	GCT,TCT	A65S	XP_016856156.1
XM_017000668.1	231	Missense Mutation	GCT,TCT	A64S	XP_016856157.1

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