BCDIN3D-AS1 BCDIN3D antisense RNA 1

Information
Symbol
BCDIN3D-AS1
Type
ncRNA
Description
BCDIN3D antisense RNA 1
Entrez Gene ID
100286844
Genome
hg19
Position
chr12:50,222,325-50,234,926
Genome
hg38
Position
chr12:49,828,542-49,841,143
HGNC
HGNC:44113 HGNC
Ensembl
ENSG00000258057 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Ranking
ClinVar
0
0
0
0
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
HGNC HGNC:44113 HGNC
Ensembl ENSG00000258057 Ensembl
AllianceGenome HGNC:44113
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000549124.1 hg38 chr12 49,828,723 49,840,204 11,482
ENST00000548872.5 hg38 chr12 49,828,542 49,841,143 12,602
ENST00000653240.1 hg38 chr12 49,828,551 49,830,730 2,180
ENST00000548872.5 hg19 chr12 50,222,325 50,234,926 12,602
ENST00000653240.1 hg19 chr12 50,222,334 50,224,513 2,180
ENST00000549124.1 hg19 chr12 50,222,506 50,233,987 11,482
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