MSANTD2-AS1 MSANTD2 antisense RNA 1

Information
Symbol
MSANTD2-AS1
Type
ncRNA
Description
MSANTD2 antisense RNA 1
Entrez Gene ID
100507283
Genome
hg19
Position
chr11:124,670,642-124,676,623
Genome
hg38
Position
chr11:124,800,746-124,806,727
HGNC
HGNC:55601 HGNC
Ensembl
ENSG00000245498 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
SYNONYM BCLET
HGNC HGNC:55601 HGNC
Ensembl ENSG00000245498 Ensembl
AllianceGenome HGNC:55601
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000664095.1 hg38 chr11 124,800,448 124,809,567 9,120
ENST00000666933.1 hg38 chr11 124,800,746 124,806,727 5,982
ENST00000667918.1 hg38 chr11 124,800,454 124,809,517 9,064
ENST00000657666.1 hg38 chr11 124,800,592 124,809,561 8,970
ENST00000664095.1 hg19 chr11 124,670,344 124,679,463 9,120
ENST00000667918.1 hg19 chr11 124,670,350 124,679,413 9,064
ENST00000657666.1 hg19 chr11 124,670,488 124,679,457 8,970
ENST00000666933.1 hg19 chr11 124,670,642 124,676,623 5,982
Genome browser