FBXW8 F-box and WD repeat domain containing 8

Information
Symbol
FBXW8
Type
protein-coding
Description
F-box and WD repeat domain containing 8
Entrez Gene ID
26259
Genome
hg19
Position
chr12:117,348,755-117,468,953
Genome
hg38
Position
chr12:116,910,950-117,031,148
MIM
609073 OMIM
HGNC
HGNC:13597 HGNC
Ensembl
ENSG00000174989 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 12
Likely benign 0 6
Uncertain significance 0 74
Ranking
ClinVar
0
0
0
92
0
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
Category :
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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 :
Filtering :
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 :
Search word :
Filtering :
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 FBW6
SYNONYM FBW8
SYNONYM FBX29
SYNONYM FBXO29
SYNONYM FBXW6
MIM 609073 OMIM
HGNC HGNC:13597 HGNC
Ensembl ENSG00000174989 Ensembl
AllianceGenome HGNC:13597
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000309909.10 hg38 chr12 116,918,693 117,029,111 110,419
ENST00000652555.1 hg38 chr12 116,910,950 117,031,148 120,199
ENST00000455858.2 hg38 chr12 116,910,965 117,031,148 120,184
ENST00000652555.1 hg19 chr12 117,348,755 117,468,953 120,199
ENST00000455858.2 hg19 chr12 117,348,770 117,468,953 120,184
ENST00000309909.10 hg19 chr12 117,356,498 117,466,916 110,419
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