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See other FCGR3A GT Assays ›
SNP ID:
rs396991
Gene
FCGR3A
Gene Name
Set Membership:
> HapMap > Validated
Chromosome Location:
Chr.1: 161544752 - 161544752 on Build GRCh38
Polymorphism:
C/A, Transversion substitution
Context Sequence [VIC/FAM]:

TCTGAAGACACATTTTTACTCCCAA[C/A]AAGCCCCCTGCAGAAGTAGGAGCCG

Assay ID C__25815666_10
Size
Availability Made To Order
Catalog # 4351379
Price
Your Price
Online offer:
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Assay Details



Species:

 Human

dbSNP Submissions:

 34 submissions

Phenotype:

 MIM: 146740

Literature Links:

 FCGR3A PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global - Not Available Caucasian
C (0.37)
(0.63)
CEPH (CEU) - Not Available
EAS - Not Available African American
C (0.38)
(0.62)
YRI (Yoruba) - Not Available
SAS - Not Available Chinese - Not Available JPT (Japanese)
T (0.22)
(0.78)
AFR - Not Available Japanese - Not Available CHB (Han Chinese)
T (0.15)
(0.85)
EUR - Not Available
AMR - Not Available
FCGR3A - Fc fragment of IgG receptor IIIa
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_001127593.1 Intron NP_001121065.1
NM_001127595.1 Intron NP_001121067.1
NM_001127596.1 Intron NP_001121068.1
XM_011509293.2 Intron XP_011507595.2

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