DDX10 DEAD-box helicase 10
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 16 |
Likely benign | 0 | 18 |
Uncertain significance | 0 | 92 |
Ranking
ClinVar | |
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0 |
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0 |
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8 |
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110 |
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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
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
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MGeND data only
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | Dbp4 |
SYNONYM | HRH-J8 |
MIM | 601235 OMIM |
HGNC | HGNC:2735 HGNC |
Ensembl | ENSG00000178105 Ensembl |
AllianceGenome | HGNC:2735 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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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 |
Key | Value |
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strand | + |
start | 108,535,751 |
Gene Symbol | DDX10 |
Entrez GeneId | 1,662 |
Chr Band | 11q22-q23 |
end | 108,811,656 |
chr | chr11 |
Name | DEAD (Asp-Glu-Ala-Asp) box polypeptide 10 |
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