CEBPA CCAAT enhancer binding protein alpha
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 1 | 76 |
Likely pathogenic | 0 | 44 |
Benign | 0 | 22 |
Likely benign | 0 | 556 |
Conflicting classifications of pathogenicity | 0 | 26 |
not provided | 59 | 12 |
Uncertain significance | 8 | 1,198 |
Ranking
ClinVar | |
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0 |
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0 |
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264 |
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1,578 |
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38 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
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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 |
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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 | C/EBP-alpha |
SYNONYM | CEBP |
MIM | 116897 OMIM |
HGNC | HGNC:1833 HGNC |
Ensembl | ENSG00000245848 Ensembl |
AllianceGenome | HGNC:1833 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000498907.3 | hg38 | chr19 | 33,299,934 | 33,302,534 | 2,601 |
ENST00000498907.3 | hg19 | chr19 | 33,790,840 | 33,793,440 | 2,601 |
Key | Value |
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strand | - |
start | 33,790,839 |
Vogelstein | TSG |
Gene Symbol | CEBPA |
Entrez GeneId | 1,050 |
Chr Band | 19q13.1 |
end | 33,793,469 |
chr | chr19 |
Name | CCAAT/enhancer binding protein (C/EBP), alpha |
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