BCL2L12 BCL2 like 12
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely pathogenic | 0 | 2 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 50 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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52 |
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2 |
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
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 |
Search Word
Target data | : |
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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MIM | 610837 OMIM |
HGNC | HGNC:13787 HGNC |
Ensembl | ENSG00000126453 Ensembl |
AllianceGenome | HGNC:13787 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000600947.5 | hg38 | chr19 | 49,665,999 | 49,673,916 | 7,918 |
ENST00000619007.4 | hg38 | chr19 | 49,665,142 | 49,673,915 | 8,774 |
ENST00000246784.8 | hg38 | chr19 | 49,665,933 | 49,673,916 | 7,984 |
ENST00000441864.6 | hg38 | chr19 | 49,665,566 | 49,673,859 | 8,294 |
ENST00000246785.7 | hg38 | chr19 | 49,665,566 | 49,673,916 | 8,351 |
ENST00000698555.1 | hg38 | chr19 | 49,665,824 | 49,673,916 | 8,093 |
ENST00000698556.1 | hg38 | chr19 | 49,665,824 | 49,673,916 | 8,093 |
ENST00000698557.1 | hg38 | chr19 | 49,665,824 | 49,673,916 | 8,093 |
ENST00000594157.5 | hg38 | chr19 | 49,665,961 | 49,673,916 | 7,956 |
ENST00000698558.1 | hg38 | chr19 | 49,665,824 | 49,673,916 | 8,093 |
ENST00000698553.1 | hg38 | chr19 | 49,665,824 | 49,673,916 | 8,093 |
ENST00000698554.1 | hg38 | chr19 | 49,665,824 | 49,673,916 | 8,093 |
ENST00000698559.1 | hg38 | chr19 | 49,665,824 | 49,673,916 | 8,093 |
ENST00000698560.1 | hg38 | chr19 | 49,665,824 | 49,673,916 | 8,093 |
ENST00000698561.1 | hg38 | chr19 | 49,665,824 | 49,673,916 | 8,093 |
ENST00000598306.2 | hg38 | chr19 | 49,666,013 | 49,673,916 | 7,904 |
ENST00000441864.6 | hg19 | chr19 | 50,168,823 | 50,177,116 | 8,294 |
ENST00000246785.7 | hg19 | chr19 | 50,168,823 | 50,177,173 | 8,351 |
ENST00000619007.4 | hg19 | chr19 | 50,168,399 | 50,177,172 | 8,774 |
ENST00000246784.8 | hg19 | chr19 | 50,169,190 | 50,177,173 | 7,984 |
ENST00000598306.2 | hg19 | chr19 | 50,169,270 | 50,177,173 | 7,904 |
ENST00000594157.5 | hg19 | chr19 | 50,169,218 | 50,177,173 | 7,956 |
ENST00000600947.5 | hg19 | chr19 | 50,169,256 | 50,177,173 | 7,918 |
ENST00000698561.1 | hg19 | chr19 | 50,169,081 | 50,177,173 | 8,093 |
ENST00000698560.1 | hg19 | chr19 | 50,169,081 | 50,177,173 | 8,093 |
ENST00000698559.1 | hg19 | chr19 | 50,169,081 | 50,177,173 | 8,093 |
ENST00000698558.1 | hg19 | chr19 | 50,169,081 | 50,177,173 | 8,093 |
ENST00000698557.1 | hg19 | chr19 | 50,169,081 | 50,177,173 | 8,093 |
ENST00000698556.1 | hg19 | chr19 | 50,169,081 | 50,177,173 | 8,093 |
ENST00000698555.1 | hg19 | chr19 | 50,169,081 | 50,177,173 | 8,093 |
ENST00000698554.1 | hg19 | chr19 | 50,169,081 | 50,177,173 | 8,093 |
ENST00000698553.1 | hg19 | chr19 | 50,169,081 | 50,177,173 | 8,093 |
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