CCNP cyclin P

Information
Symbol
CCNP
Type
protein-coding
Description
cyclin P
Entrez Gene ID
79935
Genome
hg19
Position
chr19:40,728,115-40,732,604
Genome
hg38
Position
chr19:40,222,208-40,226,697
MIM
620396 OMIM
HGNC
HGNC:25805 HGNC
Ensembl
ENSG00000105219 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 8
Uncertain significance 0 34
Ranking
ClinVar
0
0
0
42
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
SYNONYM CNTD2
MIM 620396 OMIM
HGNC HGNC:25805 HGNC
Ensembl ENSG00000105219 Ensembl
AllianceGenome HGNC:25805
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000599263.6 hg38 chr19 40,222,208 40,226,697 4,490
ENST00000430325.7 hg38 chr19 40,222,208 40,226,689 4,482
ENST00000513948.1 hg38 chr19 40,223,048 40,224,937 1,890
ENST00000430325.7 hg19 chr19 40,728,115 40,732,596 4,482
ENST00000599263.6 hg19 chr19 40,728,115 40,732,604 4,490
ENST00000513948.1 hg19 chr19 40,728,955 40,730,844 1,890
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