COIL coilin

Information
Symbol
COIL
Type
protein-coding
Description
coilin
Entrez Gene ID
8161
Genome
hg19
Position
chr17:55,015,560-55,038,411
Genome
hg38
Position
chr17:56,938,199-56,961,050
MIM
600272 OMIM
HGNC
HGNC:2184 HGNC
Ensembl
ENSG00000121058 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 8
Uncertain significance 0 48
Ranking
ClinVar
0
0
0
60
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 CLN80
SYNONYM p80-coilin
MIM 600272 OMIM
HGNC HGNC:2184 HGNC
Ensembl ENSG00000121058 Ensembl
AllianceGenome HGNC:2184
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000240316.5 hg38 chr17 56,938,199 56,961,050 22,852
ENST00000240316.5 hg19 chr17 55,015,560 55,038,411 22,852
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