DDX56 DEAD-box helicase 56

Information
Symbol
DDX56
Type
protein-coding
Description
DEAD-box helicase 56
Entrez Gene ID
54606
Genome
hg19
Position
chr7:44,605,403-44,613,507
Genome
hg38
Position
chr7:44,565,804-44,573,908
MIM
608023 OMIM
HGNC
HGNC:18193 HGNC
Ensembl
ENSG00000136271 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Likely benign 0 4
Uncertain significance 0 72
Ranking
ClinVar
0
0
0
82
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 DDX21
SYNONYM DDX26
SYNONYM NOH61
MIM 608023 OMIM
HGNC HGNC:18193 HGNC
Ensembl ENSG00000136271 Ensembl
AllianceGenome HGNC:18193
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000258772.10 hg38 chr7 44,565,804 44,573,908 8,105
ENST00000431640.5 hg38 chr7 44,566,002 44,573,925 7,924
ENST00000258772.10 hg19 chr7 44,605,403 44,613,507 8,105
ENST00000431640.5 hg19 chr7 44,605,601 44,613,524 7,924
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