BCL2L14 BCL2 like 14
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 34 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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38 |
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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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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 | BCLG |
MIM | 606126 OMIM |
HGNC | HGNC:16657 HGNC |
Ensembl | ENSG00000121380 Ensembl |
AllianceGenome | HGNC:16657 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000308721.9 | hg38 | chr12 | 12,070,939 | 12,099,695 | 28,757 |
ENST00000266434.8 | hg38 | chr12 | 12,071,468 | 12,099,695 | 28,228 |
ENST00000586576.5 | hg38 | chr12 | 12,049,861 | 12,099,684 | 49,824 |
ENST00000589718.5 | hg38 | chr12 | 12,049,844 | 12,099,684 | 49,841 |
ENST00000396367.5 | hg38 | chr12 | 12,071,468 | 12,099,695 | 28,228 |
ENST00000589718.5 | hg19 | chr12 | 12,202,778 | 12,252,618 | 49,841 |
ENST00000586576.5 | hg19 | chr12 | 12,202,795 | 12,252,618 | 49,824 |
ENST00000308721.9 | hg19 | chr12 | 12,223,873 | 12,252,629 | 28,757 |
ENST00000396367.5 | hg19 | chr12 | 12,224,402 | 12,252,629 | 28,228 |
ENST00000266434.8 | hg19 | chr12 | 12,224,402 | 12,252,629 | 28,228 |
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