TSG101 tumor susceptibility 101

Information
Symbol
TSG101
Type
protein-coding
Description
tumor susceptibility 101
Entrez Gene ID
7251
Genome
hg19
Position
chr11:18,501,858-18,548,489
Genome
hg38
Position
chr11:18,480,311-18,526,942
MIM
601387 OMIM
HGNC
HGNC:15971 HGNC
Ensembl
ENSG00000074319 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Uncertain significance 0 48
Ranking
ClinVar
0
0
0
50
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 :
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 TSG10
SYNONYM VPS23
MIM 601387 OMIM
HGNC HGNC:15971 HGNC
Ensembl ENSG00000074319 Ensembl
AllianceGenome HGNC:15971
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000251968.4 hg38 chr11 18,480,311 18,526,942 46,632
ENST00000536719.5 hg38 chr11 18,468,336 18,526,951 58,616
ENST00000536719.5 hg19 chr11 18,489,883 18,548,498 58,616
ENST00000251968.4 hg19 chr11 18,501,858 18,548,489 46,632
Genome browser