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 | |
---|---|
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0 |
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0 |
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0 |
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36 |
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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
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 |
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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 |
Search Word
Target data | : |
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 |
---|---|
SYNONYM | Dbp8 |
SYNONYM | R27090_2 |
HGNC | HGNC:18684 HGNC |
Ensembl | ENSG00000105671 Ensembl |
AllianceGenome | HGNC:18684 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
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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