BCL2L15 BCL2 like 15
Clinical Significance
MGeND | ClinVar | |
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Uncertain significance | 0 | 10 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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10 |
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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
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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 |
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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 | Bfk |
SYNONYM | C1orf178 |
MIM | 619660 OMIM |
HGNC | HGNC:33624 HGNC |
Ensembl | ENSG00000188761 Ensembl |
AllianceGenome | HGNC:33624 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000471267.1 | hg38 | chr1 | 113,881,123 | 113,887,375 | 6,253 |
ENST00000393320.3 | hg38 | chr1 | 113,881,054 | 113,887,437 | 6,384 |
ENST00000393316.8 | hg38 | chr1 | 113,876,816 | 113,887,581 | 10,766 |
ENST00000393316.8 | hg19 | chr1 | 114,419,438 | 114,430,203 | 10,766 |
ENST00000393320.3 | hg19 | chr1 | 114,423,676 | 114,430,059 | 6,384 |
ENST00000471267.1 | hg19 | chr1 | 114,423,745 | 114,429,997 | 6,253 |
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