BCL2A1 BCL2 related protein A1

Information
Symbol
BCL2A1
Type
protein-coding
Description
BCL2 related protein A1
Entrez Gene ID
597
Genome
hg19
Position
chr15:80,253,234-80,263,538
Genome
hg38
Position
chr15:79,960,892-79,971,196
MIM
601056 OMIM
HGNC
HGNC:991 HGNC
Ensembl
ENSG00000140379 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Uncertain significance 0 18
Ranking
ClinVar
0
0
0
22
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 :
Search word :
Filtering :
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 ACC-1
SYNONYM ACC-2
SYNONYM ACC1
SYNONYM ACC2
SYNONYM BCL2L5
SYNONYM BFL1
SYNONYM GRS
SYNONYM HBPA1
MIM 601056 OMIM
HGNC HGNC:991 HGNC
Ensembl ENSG00000140379 Ensembl
AllianceGenome HGNC:991
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000335661.6 hg38 chr15 79,960,892 79,971,169 10,278
ENST00000677151.1 hg38 chr15 79,970,541 79,971,196 656
ENST00000267953.4 hg38 chr15 79,960,892 79,971,196 10,305
ENST00000335661.6 hg19 chr15 80,253,234 80,263,511 10,278
ENST00000267953.4 hg19 chr15 80,253,234 80,263,538 10,305
ENST00000677151.1 hg19 chr15 80,262,883 80,263,538 656
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