DDX49 DEAD-box helicase 49

Information
Symbol
DDX49
Type
protein-coding
Description
DEAD-box helicase 49
Entrez Gene ID
54555
Genome
hg19
Position
chr19:19,030,524-19,039,439
Genome
hg38
Position
chr19:18,919,715-18,928,630
HGNC
HGNC:18684 HGNC
Ensembl
ENSG00000105671 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 6
Uncertain significance 0 30
Ranking
ClinVar
0
0
0
36
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 Dbp8
SYNONYM R27090_2
HGNC HGNC:18684 HGNC
Ensembl ENSG00000105671 Ensembl
AllianceGenome HGNC:18684
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000247003.9 hg38 chr19 18,919,715 18,928,630 8,916
ENST00000247003.9 hg19 chr19 19,030,524 19,039,439 8,916
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