BCL2L15 BCL2 like 15

Information
Symbol
BCL2L15
Type
protein-coding
Description
BCL2 like 15
Entrez Gene ID
440603
Genome
hg19
Position
chr1:114,419,438-114,430,203
Genome
hg38
Position
chr1:113,876,816-113,887,581
MIM
619660 OMIM
HGNC
HGNC:33624 HGNC
Ensembl
ENSG00000188761 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 10
Ranking
ClinVar
0
0
0
10
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
Target data :
MGeND data only
Category :
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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
SYNONYM Bfk
SYNONYM C1orf178
MIM 619660 OMIM
HGNC HGNC:33624 HGNC
Ensembl ENSG00000188761 Ensembl
AllianceGenome HGNC:33624
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
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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