THOC5 THO complex subunit 5

Information
Symbol
THOC5
Type
protein-coding
Description
THO complex subunit 5
Entrez Gene ID
8563
Genome
hg19
Position
chr22:29,901,868-29,949,746
Genome
hg38
Position
chr22:29,505,879-29,553,757
MIM
612733 OMIM
HGNC
HGNC:19074 HGNC
Ensembl
ENSG00000100296 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Uncertain significance 0 40
Ranking
ClinVar
0
0
0
44
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 C22orf19
SYNONYM Fmip
SYNONYM PK1.3
SYNONYM fSAP79
MIM 612733 OMIM
HGNC HGNC:19074 HGNC
Ensembl ENSG00000100296 Ensembl
AllianceGenome HGNC:19074
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000397872.5 hg38 chr22 29,508,168 29,553,655 45,488
ENST00000397871.5 hg38 chr22 29,508,168 29,553,655 45,488
ENST00000397873.6 hg38 chr22 29,508,358 29,553,766 45,409
ENST00000490103.6 hg38 chr22 29,505,879 29,553,757 47,879
ENST00000397871.5 hg19 chr22 29,904,157 29,949,644 45,488
ENST00000397872.5 hg19 chr22 29,904,157 29,949,644 45,488
ENST00000490103.6 hg19 chr22 29,901,868 29,949,746 47,879
ENST00000397873.6 hg19 chr22 29,904,347 29,949,755 45,409
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