JTB jumping translocation breakpoint

Information
Symbol
JTB
Type
protein-coding
Description
jumping translocation breakpoint
Entrez Gene ID
10899
Genome
hg19
Position
chr1:153,946,745-153,950,150
Genome
hg38
Position
chr1:153,974,269-153,977,674
MIM
604671 OMIM
HGNC
HGNC:6201 HGNC
Ensembl
ENSG00000143543 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Uncertain significance 0 10
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 :
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 HJTB
SYNONYM HSPC222
SYNONYM PAR
SYNONYM hJT
MIM 604671 OMIM
HGNC HGNC:6201 HGNC
Ensembl ENSG00000143543 Ensembl
AllianceGenome HGNC:6201
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000271843.9 hg38 chr1 153,974,269 153,977,674 3,406
ENST00000356648.5 hg38 chr1 153,974,512 153,977,638 3,127
ENST00000368589.5 hg38 chr1 153,974,512 153,977,660 3,149
ENST00000271843.9 hg19 chr1 153,946,745 153,950,150 3,406
ENST00000356648.5 hg19 chr1 153,946,988 153,950,114 3,127
ENST00000368589.5 hg19 chr1 153,946,988 153,950,136 3,149
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