CDC27 cell division cycle 27

Information
Symbol
CDC27
Type
protein-coding
Description
cell division cycle 27
Entrez Gene ID
996
Genome
hg19
Position
chr17:45,197,621-45,266,542
Genome
hg38
Position
chr17:47,120,255-47,189,176
MIM
116946 OMIM
HGNC
HGNC:1728 HGNC
Ensembl
ENSG00000004897 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 2
Benign 0 2
Likely benign 0 6
Uncertain significance 0 4
Ranking
ClinVar
0
0
2
6
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 ANAPC3
SYNONYM APC3
SYNONYM CDC27Hs
SYNONYM D0S1430E
SYNONYM D17S978E
SYNONYM H-NUC
SYNONYM HNUC
SYNONYM NUC2
MIM 116946 OMIM
HGNC HGNC:1728 HGNC
Ensembl ENSG00000004897 Ensembl
AllianceGenome HGNC:1728
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000527547.5 hg38 chr17 47,120,880 47,189,224 68,345
ENST00000531206.5 hg38 chr17 47,120,255 47,189,176 68,922
ENST00000066544.8 hg38 chr17 47,117,703 47,189,295 71,593
ENST00000066544.8 hg19 chr17 45,195,069 45,266,661 71,593
ENST00000531206.5 hg19 chr17 45,197,621 45,266,542 68,922
ENST00000527547.5 hg19 chr17 45,198,246 45,266,590 68,345
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