CKLF-CMTM1 CKLF-CMTM1 readthrough

Information
Symbol
CKLF-CMTM1
Type
protein-coding
Description
CKLF-CMTM1 readthrough
Entrez Gene ID
100529251
Genome
hg19
Position
chr16:66,586,582-66,613,038
Genome
hg38
Position
chr16:66,552,679-66,579,135
HGNC
HGNC:39977 HGNC
Ensembl
ENSG00000254788 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 6
Uncertain significance 0 30
Ranking
ClinVar
0
0
0
38
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 :
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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
HGNC HGNC:39977 HGNC
Ensembl ENSG00000254788 Ensembl
AllianceGenome HGNC:39977
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000532838.1 hg38 chr16 66,552,649 66,566,428 13,780
ENST00000527729.5 hg38 chr16 66,552,613 66,579,135 26,523
ENST00000615332.5 hg38 chr16 66,552,679 66,578,931 26,253
ENST00000616804.5 hg38 chr16 66,552,679 66,579,135 26,457
ENST00000527729.5 hg19 chr16 66,586,516 66,613,038 26,523
ENST00000532838.1 hg19 chr16 66,586,552 66,600,331 13,780
ENST00000615332.5 hg19 chr16 66,586,582 66,612,834 26,253
ENST00000616804.5 hg19 chr16 66,586,582 66,613,038 26,457
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