DHX33 DEAH-box helicase 33

Information
Symbol
DHX33
Type
protein-coding
Description
DEAH-box helicase 33
Entrez Gene ID
56919
Genome
hg19
Position
chr17:5,344,237-5,372,302
Genome
hg38
Position
chr17:5,440,917-5,468,982
MIM
614405 OMIM
HGNC
HGNC:16718 HGNC
Ensembl
ENSG00000005100 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 90
Ranking
ClinVar
0
0
0
90
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
SYNONYM DDX33
MIM 614405 OMIM
HGNC HGNC:16718 HGNC
Ensembl ENSG00000005100 Ensembl
AllianceGenome HGNC:16718
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000433302.7 hg38 chr17 5,443,489 5,468,916 25,428
ENST00000225296.8 hg38 chr17 5,440,917 5,468,982 28,066
ENST00000225296.8 hg19 chr17 5,344,237 5,372,302 28,066
ENST00000433302.7 hg19 chr17 5,346,809 5,372,236 25,428
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