DDX10 DEAD-box helicase 10

Information
Symbol
DDX10
Type
protein-coding
Description
DEAD-box helicase 10
Entrez Gene ID
1662
Genome
hg19
Position
chr11:108,535,796-108,811,654
Genome
hg38
Position
chr11:108,665,069-108,940,927
MIM
601235 OMIM
HGNC
HGNC:2735 HGNC
Ensembl
ENSG00000178105 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 16
Likely benign 0 18
Uncertain significance 0 92
Ranking
ClinVar
0
0
8
110
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
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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 :
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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 Dbp4
SYNONYM HRH-J8
MIM 601235 OMIM
HGNC HGNC:2735 HGNC
Ensembl ENSG00000178105 Ensembl
AllianceGenome HGNC:2735
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000322536.8 hg38 chr11 108,665,069 108,940,927 275,859
ENST00000526794.1 hg38 chr11 108,665,122 108,922,243 257,122
ENST00000686283.1 hg38 chr11 108,665,069 108,940,999 275,931
ENST00000322536.8 hg19 chr11 108,535,796 108,811,654 275,859
ENST00000526794.1 hg19 chr11 108,535,849 108,792,970 257,122
ENST00000686283.1 hg19 chr11 108,535,796 108,811,726 275,931
KeyValue
strand+
start108,535,751
Gene SymbolDDX10
Entrez GeneId1,662
Chr Band11q22-q23
end108,811,656
chrchr11
NameDEAD (Asp-Glu-Ala-Asp) box polypeptide 10
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