CGN cingulin

Information
Symbol
CGN
Type
protein-coding
Description
cingulin
Entrez Gene ID
57530
Genome
hg19
Position
chr1:151,483,863-151,511,168
Genome
hg38
Position
chr1:151,511,387-151,538,692
MIM
609473 OMIM
HGNC
HGNC:17429 HGNC
Ensembl
ENSG00000143375 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 10
Likely benign 0 16
Uncertain significance 0 158
Ranking
ClinVar
0
0
4
178
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
MIM 609473 OMIM
HGNC HGNC:17429 HGNC
Ensembl ENSG00000143375 Ensembl
AllianceGenome HGNC:17429
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000271636.12 hg38 chr1 151,511,387 151,538,692 27,306
ENST00000271636.12 hg19 chr1 151,483,863 151,511,168 27,306
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