DCAF4 DDB1 and CUL4 associated factor 4
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 4 |
| Likely benign | 0 | 12 |
| Uncertain significance | 0 | 68 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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82 |
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2 |
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
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| Filtering | : |
| 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
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | WDR21 |
| SYNONYM | WDR21A |
| MIM | 616372 OMIM |
| HGNC | HGNC:20229 HGNC |
| Ensembl | ENSG00000119599 Ensembl |
| AllianceGenome | HGNC:20229 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000394234.6 | hg38 | chr14 | 72,926,478 | 72,959,703 | 33,226 |
| ENST00000553457.1 | hg38 | chr14 | 72,937,989 | 72,958,112 | 20,124 |
| ENST00000509153.5 | hg38 | chr14 | 72,926,480 | 72,958,946 | 32,467 |
| ENST00000358377.7 | hg38 | chr14 | 72,926,464 | 72,959,703 | 33,240 |
| ENST00000353777.7 | hg38 | chr14 | 72,926,377 | 72,959,592 | 33,216 |
| ENST00000555042.5 | hg38 | chr14 | 72,926,487 | 72,959,644 | 33,158 |
| ENST00000353777.7 | hg19 | chr14 | 73,393,085 | 73,426,300 | 33,216 |
| ENST00000358377.7 | hg19 | chr14 | 73,393,172 | 73,426,411 | 33,240 |
| ENST00000394234.6 | hg19 | chr14 | 73,393,186 | 73,426,411 | 33,226 |
| ENST00000509153.5 | hg19 | chr14 | 73,393,188 | 73,425,654 | 32,467 |
| ENST00000555042.5 | hg19 | chr14 | 73,393,195 | 73,426,352 | 33,158 |
| ENST00000553457.1 | hg19 | chr14 | 73,404,697 | 73,424,820 | 20,124 |
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