DDX39B DExD-box helicase 39B

Information
Symbol
DDX39B
Type
protein-coding
Description
DExD-box helicase 39B
Entrez Gene ID
7919
Genome
hg19
Position
chr6:31,497,996-31,510,225
Genome
hg38
Position
chr6:31,530,219-31,542,448
MIM
142560 OMIM
HGNC
HGNC:13917 HGNC
Ensembl
ENSG00000198563 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
not provided 18 0
Uncertain significance 0 24
Ranking
ClinVar
0
0
0
30
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
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 BAT1
SYNONYM D6S81E
SYNONYM UAP56
MIM 142560 OMIM
HGNC HGNC:13917 HGNC
Ensembl ENSG00000198563 Ensembl
AllianceGenome HGNC:13917
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000376177.6 hg38 chr6 31,530,219 31,540,536 10,318
ENST00000458640.5 hg38 chr6 31,530,219 31,542,448 12,230
ENST00000396172.6 hg38 chr6 31,530,226 31,542,003 11,778
ENST00000376177.6 hg19 chr6 31,497,996 31,508,313 10,318
ENST00000396172.6 hg19 chr6 31,498,003 31,509,780 11,778
ENST00000458640.5 hg19 chr6 31,497,996 31,510,225 12,230
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