DCAF7 DDB1 and CUL4 associated factor 7
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Uncertain significance | 0 | 6 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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12 |
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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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Filtering | : |
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 | AN11 |
SYNONYM | HAN11 |
SYNONYM | SWAN-1 |
SYNONYM | WDR68 |
MIM | 605973 OMIM |
HGNC | HGNC:30915 HGNC |
Ensembl | ENSG00000136485 Ensembl |
AllianceGenome | HGNC:30915 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000615512.2 | hg38 | chr17 | 63,550,509 | 63,594,259 | 43,751 |
ENST00000688888.1 | hg38 | chr17 | 63,550,539 | 63,592,218 | 41,680 |
ENST00000692877.1 | hg38 | chr17 | 63,550,614 | 63,592,232 | 41,619 |
ENST00000614556.5 | hg38 | chr17 | 63,550,477 | 63,594,266 | 43,790 |
ENST00000688437.1 | hg38 | chr17 | 63,550,501 | 63,594,266 | 43,766 |
ENST00000582274.2 | hg38 | chr17 | 63,550,510 | 63,553,190 | 2,681 |
ENST00000415273.2 | hg38 | chr17 | 63,550,500 | 63,589,785 | 39,286 |
ENST00000691063.1 | hg38 | chr17 | 63,550,482 | 63,594,286 | 43,805 |
ENST00000690481.1 | hg38 | chr17 | 63,550,477 | 63,586,114 | 35,638 |
ENST00000415273.2 | hg19 | chr17 | 61,627,861 | 61,667,147 | 39,287 |
ENST00000582274.2 | hg19 | chr17 | 61,627,871 | 61,630,551 | 2,681 |
ENST00000614556.5 | hg19 | chr17 | 61,627,838 | 61,671,628 | 43,791 |
ENST00000615512.2 | hg19 | chr17 | 61,627,870 | 61,671,621 | 43,752 |
ENST00000688437.1 | hg19 | chr17 | 61,627,862 | 61,671,628 | 43,767 |
ENST00000688888.1 | hg19 | chr17 | 61,627,900 | 61,669,580 | 41,681 |
ENST00000690481.1 | hg19 | chr17 | 61,627,838 | 61,663,476 | 35,639 |
ENST00000691063.1 | hg19 | chr17 | 61,627,843 | 61,671,648 | 43,806 |
ENST00000692877.1 | hg19 | chr17 | 61,627,975 | 61,669,594 | 41,620 |
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