EFCAB13-DT EFCAB13 divergent transcript

Information
Symbol
EFCAB13-DT
Type
ncRNA
Description
EFCAB13 divergent transcript
Entrez Gene ID
102724508
Genome
hg19
Position
chr17:45,400,558-45,401,267
Genome
hg38
Position
chr17:47,323,192-47,323,901
HGNC
HGNC:55338 HGNC
Ensembl
ENSG00000263293 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Ranking
ClinVar
0
0
0
0
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 THCAT158
HGNC HGNC:55338 HGNC
Ensembl ENSG00000263293 Ensembl
AllianceGenome HGNC:55338
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000702530.1 hg38 chr17 47,323,192 47,323,901 710
ENST00000576345.2 hg38 chr17 47,303,460 47,305,685 2,226
ENST00000575039.1 hg38 chr17 47,303,474 47,323,613 20,140
ENST00000576345.2 hg19 chr17 45,380,826 45,383,051 2,226
ENST00000575039.1 hg19 chr17 45,380,840 45,400,979 20,140
ENST00000702530.1 hg19 chr17 45,400,558 45,401,267 710
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