TNS2 tensin 2

Information
Symbol
TNS2
Type
protein-coding
Description
tensin 2
Entrez Gene ID
23371
Genome
hg19
Position
chr12:53,442,733-53,458,155
Genome
hg38
Position
chr12:53,048,949-53,064,371
MIM
607717 OMIM
HGNC
HGNC:19737 HGNC
Ensembl
ENSG00000111077 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 102
Likely benign 0 222
Conflicting classifications of pathogenicity 0 14
Uncertain significance 0 376
Ranking
ClinVar
0
0
126
546
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 :
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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 C1-TEN
SYNONYM C1TEN
SYNONYM TENC1
MIM 607717 OMIM
HGNC HGNC:19737 HGNC
Ensembl ENSG00000111077 Ensembl
AllianceGenome HGNC:19737
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000546602.5 hg38 chr12 53,050,186 53,064,372 14,187
ENST00000552570.5 hg38 chr12 53,050,186 53,064,372 14,187
ENST00000314276.7 hg38 chr12 53,048,949 53,064,371 15,423
ENST00000379902.7 hg38 chr12 53,046,969 53,064,369 17,401
ENST00000549700.5 hg38 chr12 53,050,186 53,064,372 14,187
ENST00000314250.11 hg38 chr12 53,050,065 53,064,379 14,315
ENST00000314276.7 hg19 chr12 53,442,733 53,458,155 15,423
ENST00000379902.7 hg19 chr12 53,440,753 53,458,153 17,401
ENST00000314250.11 hg19 chr12 53,443,849 53,458,163 14,315
ENST00000546602.5 hg19 chr12 53,443,970 53,458,156 14,187
ENST00000549700.5 hg19 chr12 53,443,970 53,458,156 14,187
ENST00000552570.5 hg19 chr12 53,443,970 53,458,156 14,187
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