BCL2L12 BCL2 like 12

Information
Symbol
BCL2L12
Type
protein-coding
Description
BCL2 like 12
Entrez Gene ID
83596
Genome
hg19
Position
chr19:50,168,823-50,177,173
Genome
hg38
Position
chr19:49,665,566-49,673,916
MIM
610837 OMIM
HGNC
HGNC:13787 HGNC
Ensembl
ENSG00000126453 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely pathogenic 0 2
Likely benign 0 2
Uncertain significance 0 50
Ranking
ClinVar
0
0
0
52
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
Category :
Search word :
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Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
MIM 610837 OMIM
HGNC HGNC:13787 HGNC
Ensembl ENSG00000126453 Ensembl
AllianceGenome HGNC:13787
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
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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