TSSC4 tumor suppressing subtransferable candidate 4

Information
Symbol
TSSC4
Type
protein-coding
Description
tumor suppressing subtransferable candidate 4
Entrez Gene ID
10078
Genome
hg19
Position
chr11:2,421,980-2,425,106
Genome
hg38
Position
chr11:2,400,750-2,403,876
MIM
603852 OMIM
HGNC
HGNC:12386 HGNC
Ensembl
ENSG00000184281 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 4
Uncertain significance 0 60
Ranking
ClinVar
0
0
0
68
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
MIM 603852 OMIM
HGNC HGNC:12386 HGNC
Ensembl ENSG00000184281 Ensembl
AllianceGenome HGNC:12386
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000380992.5 hg38 chr11 2,400,628 2,403,701 3,074
ENST00000380996.9 hg38 chr11 2,400,488 2,403,878 3,391
ENST00000333256.11 hg38 chr11 2,400,750 2,403,876 3,127
ENST00000451491.2 hg38 chr11 2,402,293 2,403,875 1,583
ENST00000380996.9 hg19 chr11 2,421,718 2,425,108 3,391
ENST00000380992.5 hg19 chr11 2,421,858 2,424,931 3,074
ENST00000333256.11 hg19 chr11 2,421,980 2,425,106 3,127
ENST00000451491.2 hg19 chr11 2,423,523 2,425,105 1,583
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