Product Details

SNP ID

rs199737051

Assay Type

Functionally tested

NCBI dbSNP Submissions

2

Location

Chr.1:161509829 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TATTTGTGTCTTTCAGAATGGCTGG[G/T]GCTCCAGACCCCTCACCTGGAGTTC

Phenotype

MIM: 146790

Polymorphism

G/T, Transversion substitution

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	412	Missense Mutation	GGG,GTG	G125V	NP_001129691.1
NM_021642.3	412	Missense Mutation	GGG,GTG	G124V	NP_067674.2
XM_011509287.2	412	Missense Mutation	GGG,GTG	G125V	XP_011507589.1
XM_011509290.2	412	Missense Mutation	GGG,GTG	G125V	XP_011507592.1
XM_011509291.1	412	Missense Mutation	GGG,GTG	G125V	XP_011507593.1
XM_017000663.1	412	Missense Mutation	GGG,GTG	G124V	XP_016856152.1
XM_017000664.1	412	Missense Mutation	GGG,GTG	G125V	XP_016856153.1
XM_017000665.1	412	Missense Mutation	GGG,GTG	G125V	XP_016856154.1
XM_017000666.1	412	Missense Mutation	GGG,GTG	G125V	XP_016856155.1
XM_017000667.1	412	Missense Mutation	GGG,GTG	G125V	XP_016856156.1
XM_017000668.1	412	Missense Mutation	GGG,GTG	G124V	XP_016856157.1

View Full Product Details