DDX19A DEAD-box helicase 19A

Information
Symbol
DDX19A
Type
protein-coding
Description
DEAD-box helicase 19A
Entrez Gene ID
55308
Genome
hg19
Position
chr16:70,380,806-70,407,286
Genome
hg38
Position
chr16:70,346,903-70,373,383
HGNC
HGNC:25628 HGNC
Ensembl
ENSG00000168872 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 32
Ranking
ClinVar
0
0
0
34
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 DDX19-DDX19L
SYNONYM DDX19L
HGNC HGNC:25628 HGNC
Ensembl ENSG00000168872 Ensembl
AllianceGenome HGNC:25628
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000302243.12 hg38 chr16 70,346,903 70,373,383 26,481
ENST00000417604.6 hg38 chr16 70,346,944 70,372,297 25,354
ENST00000302243.12 hg19 chr16 70,380,806 70,407,286 26,481
ENST00000417604.6 hg19 chr16 70,380,847 70,406,200 25,354
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