BCL3 BCL3 transcription coactivator
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 62 |
Ranking
ClinVar | |
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0 |
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0 |
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4 |
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66 |
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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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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 |
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MGeND data only
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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 | BCL4 |
SYNONYM | D19S37 |
MIM | 109560 OMIM |
HGNC | HGNC:998 HGNC |
Ensembl | ENSG00000069399 Ensembl |
AllianceGenome | HGNC:998 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000164227.10 | hg38 | chr19 | 44,748,708 | 44,760,044 | 11,337 |
ENST00000164227.10 | hg19 | chr19 | 45,251,965 | 45,263,301 | 11,337 |
Key | Value |
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strand | + |
UniProt | OG |
start | 45,251,977 |
Gene Symbol | BCL3 |
Entrez GeneId | 602 |
Chr Band | 19q13 |
end | 45,263,300 |
chr | chr19 |
Name | B-cell CLL/lymphoma 3 |
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