TCTA T cell leukemia translocation altered

Information
Symbol
TCTA
Type
protein-coding
Description
T cell leukemia translocation altered
Entrez Gene ID
6988
Genome
hg19
Position
chr3:49,449,856-49,453,909
Genome
hg38
Position
chr3:49,412,423-49,416,476
MIM
600690 OMIM
HGNC
HGNC:11692 HGNC
Ensembl
ENSG00000145022 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 12
Ranking
ClinVar
0
0
0
12
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
MIM 600690 OMIM
HGNC HGNC:11692 HGNC
Ensembl ENSG00000145022 Ensembl
AllianceGenome HGNC:11692
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000273590.4 hg38 chr3 49,412,423 49,416,476 4,054
ENST00000273590.4 hg19 chr3 49,449,856 49,453,909 4,054
KeyValue
strand+
UniProtOG
start49,449,638
Gene SymbolTCTA
Entrez GeneId6,988
Chr Band3p21
end49,453,908
chrchr3
Genome browser