FCGR3B Fc gamma receptor IIIb

Information
Symbol
FCGR3B
Type
protein-coding
Description
Fc gamma receptor IIIb
Entrez Gene ID
2215
Genome
hg19
Position
chr1:161,592,986-161,601,753
Genome
hg38
Position
chr1:161,623,196-161,631,963
MIM
610665 OMIM
HGNC
HGNC:3620 HGNC
Ensembl
ENSG00000162747 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Likely benign 0 6
Uncertain significance 0 30
Ranking
ClinVar
0
0
0
40
2
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
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Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
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Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
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Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM CD16
SYNONYM CD16-I
SYNONYM CD16A
SYNONYM CD16b
SYNONYM FCG3
SYNONYM FCGR3
SYNONYM FCGR3A
SYNONYM FCR-10
SYNONYM FCRIII
SYNONYM FCRIIIb
MIM 610665 OMIM
HGNC HGNC:3620 HGNC
Ensembl ENSG00000162747 Ensembl
AllianceGenome HGNC:3620
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000421702.4 hg38 chr1 161,623,418 161,631,180 7,763
ENST00000650385.1 hg38 chr1 161,623,196 161,631,176 7,981
ENST00000367964.6 hg38 chr1 161,623,196 161,631,963 8,768
ENST00000650385.1 hg19 chr1 161,592,986 161,600,966 7,981
ENST00000367964.6 hg19 chr1 161,592,986 161,601,753 8,768
ENST00000421702.4 hg19 chr1 161,593,208 161,600,970 7,763
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