CCPG1 cell cycle progression 1

Go to:

Information
Clinical Significance
Ranking
Frequency
Disease area statistics
Locus Zoom
Variants
Genome browser

Information

Symbol: CCPG1
Type: protein-coding
Description: cell cycle progression 1
Entrez Gene ID: 9236
Genome: hg19
Position: chr15:55,647,437-55,700,557
Genome: hg38
Position: chr15:55,355,239-55,408,359
MIM: 611326 OMIM
HGNC: HGNC:24227 HGNC
Ensembl: ENSG00000260916 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Pathogenic	0	2
Likely pathogenic	0	2
Benign	0	4
Likely benign	0	24
Uncertain significance	0	96

Ranking

	ClinVar
	0
	0
	8
	118
	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
Variant name	Gene	AA change	CDS	Japanese frequency	TogoVar	Entry	Origin	Type	Annotation	Genome	Entry	Origin	Annotation	CIViC evidence	DisGeNET entry	COSMIC occurrence	Prediction

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
Name	Entry	Origin	Type	Annotation	Type	Genome	Size	Chromosome	Start	Stop	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry

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
Name	Entry	Origin	Type	Annotation	Type	Genome	Gene symbol	Chromosome	Genomic start	Genomic stop	Strand	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry

Type	ID
SYNONYM	CPR8
MIM	611326 OMIM
HGNC	HGNC:24227 HGNC
Ensembl	ENSG00000260916 Ensembl
AllianceGenome	HGNC:24227

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000442196.8	hg38	chr15	55,355,239	55,408,359	53,121
ENST00000569205.5	hg38	chr15	55,359,018	55,408,052	49,035
ENST00000310958.10	hg38	chr15	55,355,250	55,408,510	53,261
ENST00000425574.7	hg38	chr15	55,355,645	55,408,306	52,662
ENST00000442196.8	hg19	chr15	55,647,437	55,700,557	53,121
ENST00000310958.10	hg19	chr15	55,647,448	55,700,708	53,261
ENST00000425574.7	hg19	chr15	55,647,843	55,700,504	52,662
ENST00000569205.5	hg19	chr15	55,651,216	55,700,250	49,035

Genome browser