BECN1 beclin 1

Information
Symbol
BECN1
Type
protein-coding
Description
beclin 1
Entrez Gene ID
8678
Genome
hg19
Position
chr17:40,962,152-40,976,281
Genome
hg38
Position
chr17:42,810,134-42,824,263
MIM
604378 OMIM
HGNC
HGNC:1034 HGNC
Ensembl
ENSG00000126581 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 4
Uncertain significance 0 30
Ranking
ClinVar
0
0
0
36
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 :
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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 ATG6
SYNONYM VPS30
SYNONYM beclin1
MIM 604378 OMIM
HGNC HGNC:1034 HGNC
Ensembl ENSG00000126581 Ensembl
AllianceGenome HGNC:1034
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000361523.8 hg38 chr17 42,810,134 42,824,263 14,130
ENST00000438274.7 hg38 chr17 42,810,308 42,824,287 13,980
ENST00000590099.6 hg38 chr17 42,810,134 42,824,282 14,149
ENST00000361523.8 hg19 chr17 40,962,152 40,976,281 14,130
ENST00000438274.7 hg19 chr17 40,962,326 40,976,305 13,980
ENST00000590099.6 hg19 chr17 40,962,152 40,976,300 14,149
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