FBXW10 F-box and WD repeat domain containing 10

Information
Symbol
FBXW10
Type
protein-coding
Description
F-box and WD repeat domain containing 10
Entrez Gene ID
10517
Genome
hg19
Position
chr17:18,647,339-18,682,662
Genome
hg38
Position
chr17:18,744,026-18,779,349
MIM
611679 OMIM
HGNC
HGNC:1211 HGNC
Ensembl
ENSG00000171931 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 2
not provided 2 0
Ranking
ClinVar
0
0
0
4
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
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
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 Fbw10
SYNONYM HREP
SYNONYM SM25H2
SYNONYM SM2SH2
MIM 611679 OMIM
HGNC HGNC:1211 HGNC
Ensembl ENSG00000171931 Ensembl
AllianceGenome HGNC:1211
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000301938.4 hg38 chr17 18,744,075 18,779,349 35,275
ENST00000308799.8 hg38 chr17 18,744,026 18,779,349 35,324
ENST00000395665.9 hg38 chr17 18,744,054 18,779,349 35,296
ENST00000308799.8 hg19 chr17 18,647,339 18,682,662 35,324
ENST00000395665.9 hg19 chr17 18,647,367 18,682,662 35,296
ENST00000301938.4 hg19 chr17 18,647,388 18,682,662 35,275
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