CAPG capping actin protein, gelsolin like

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

Symbol: CAPG
Type: protein-coding
Description: capping actin protein, gelsolin like
Entrez Gene ID: 822
Genome: hg19
Position: chr2:85,621,876-85,637,489
Genome: hg38
Position: chr2:85,394,753-85,410,366
MIM: 153615 OMIM
HGNC: HGNC:1474 HGNC
Ensembl: ENSG00000042493 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	6
Likely benign	0	4
not provided	0	2
Uncertain significance	0	24

Ranking

	ClinVar
	0
	0
	0
	34
	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
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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
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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
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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	AFCP
SYNONYM	HEL-S-66
SYNONYM	MCP
MIM	153615 OMIM
HGNC	HGNC:1474 HGNC
Ensembl	ENSG00000042493 Ensembl
AllianceGenome	HGNC:1474

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000409724.5	hg38	chr2	85,394,893	85,414,074	19,182
ENST00000409921.5	hg38	chr2	85,394,767	85,410,370	15,604
ENST00000409670.5	hg38	chr2	85,394,828	85,414,042	19,215
ENST00000263867.9	hg38	chr2	85,394,753	85,410,366	15,614
ENST00000263867.9	hg19	chr2	85,621,876	85,637,489	15,614
ENST00000409921.5	hg19	chr2	85,621,890	85,637,493	15,604
ENST00000409670.5	hg19	chr2	85,621,951	85,641,165	19,215
ENST00000409724.5	hg19	chr2	85,622,016	85,641,197	19,182

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