DEPDC4 DEP domain containing 4
Information
- Symbol
- DEPDC4
- Type
- protein-coding
- Description
- DEP domain containing 4
- Entrez Gene ID
- 120863
- Genome
- hg19
- Position
- chr12:100,633,840-100,660,857
- Genome
- hg38
- Position
- chr12:100,240,062-100,267,079
- HGNC
- HGNC:22952 HGNC
- Ensembl
- ENSG00000166153 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
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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32 |
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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 |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
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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Category | : |
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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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000550587.6 | hg38 | chr12 | 100,240,062 | 100,267,079 | 27,018 |
ENST00000416321.5 | hg38 | chr12 | 100,252,263 | 100,267,079 | 14,817 |
ENST00000550587.6 | hg19 | chr12 | 100,633,840 | 100,660,857 | 27,018 |
ENST00000416321.5 | hg19 | chr12 | 100,646,041 | 100,660,857 | 14,817 |
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