CD27 CD27 molecule

Information
Symbol
CD27
Type
protein-coding
Description
CD27 molecule
Entrez Gene ID
939
Genome
hg19
Position
chr12:6,554,121-6,560,879
Genome
hg38
Position
chr12:6,444,955-6,451,713
MIM
186711 OMIM
HGNC
HGNC:11922 HGNC
Ensembl
ENSG00000139193 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 18
Likely pathogenic 0 8
Benign 0 18
Likely benign 0 152
Conflicting classifications of pathogenicity 0 8
Uncertain significance 0 192
Ranking
ClinVar
0
0
48
332
4
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 S152
SYNONYM S152. LPFS2
SYNONYM T14
SYNONYM TNFRSF7
SYNONYM Tp55
MIM 186711 OMIM
HGNC HGNC:11922 HGNC
Ensembl ENSG00000139193 Ensembl
AllianceGenome HGNC:11922
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000266557.4 hg38 chr12 6,444,955 6,451,713 6,759
ENST00000266557.4 hg19 chr12 6,554,121 6,560,879 6,759
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