CCIN calicin

Information
Symbol
CCIN
Type
protein-coding
Description
calicin
Entrez Gene ID
881
Genome
hg19
Position
chr9:36,169,385-36,171,331
Genome
hg38
Position
chr9:36,169,388-36,171,334
MIM
603960 OMIM
HGNC
HGNC:1568 HGNC
Ensembl
ENSG00000185972 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 10
Benign 0 2
Uncertain significance 0 68
Ranking
ClinVar
0
0
0
70
10
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 :
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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 BTBD20
SYNONYM KBTBD14
SYNONYM SPGF91
MIM 603960 OMIM
HGNC HGNC:1568 HGNC
Ensembl ENSG00000185972 Ensembl
AllianceGenome HGNC:1568
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000335119.4 hg38 chr9 36,169,388 36,171,334 1,947
ENST00000335119.4 hg19 chr9 36,169,385 36,171,331 1,947
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