CASC16 cancer susceptibility 16

Information
Symbol
CASC16
Type
ncRNA
Description
cancer susceptibility 16
Entrez Gene ID
643714
Genome
hg19
Position
chr16:52,585,996-52,640,897
Genome
hg38
Position
chr16:52,552,084-52,606,985
HGNC
HGNC:48608 HGNC
Ensembl
ENSG00000249231 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 LINC00918
HGNC HGNC:48608 HGNC
Ensembl ENSG00000249231 Ensembl
AllianceGenome HGNC:48608
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000652959.1 hg38 chr16 52,552,182 52,652,132 99,951
ENST00000510238.8 hg38 chr16 52,552,084 52,606,985 54,902
ENST00000510238.8 hg19 chr16 52,585,996 52,640,897 54,902
ENST00000652959.1 hg19 chr16 52,586,094 52,686,044 99,951
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