COPE COPI coat complex subunit epsilon
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 36 |
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
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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 |
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 |
Type | ID |
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SYNONYM | epsilon-COP |
MIM | 606942 OMIM |
HGNC | HGNC:2234 HGNC |
Ensembl | ENSG00000105669 Ensembl |
AllianceGenome | HGNC:2234 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000349893.8 | hg38 | chr19 | 18,899,517 | 18,919,363 | 19,847 |
ENST00000262812.9 | hg38 | chr19 | 18,899,514 | 18,919,387 | 19,874 |
ENST00000351079.8 | hg38 | chr19 | 18,899,573 | 18,919,375 | 19,803 |
ENST00000600932.5 | hg38 | chr19 | 18,899,563 | 18,919,380 | 19,818 |
ENST00000262812.9 | hg19 | chr19 | 19,010,323 | 19,030,196 | 19,874 |
ENST00000349893.8 | hg19 | chr19 | 19,010,326 | 19,030,172 | 19,847 |
ENST00000600932.5 | hg19 | chr19 | 19,010,372 | 19,030,189 | 19,818 |
ENST00000351079.8 | hg19 | chr19 | 19,010,382 | 19,030,184 | 19,803 |
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