ARHGAP35 Rho GTPase activating protein 35

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: ARHGAP35
Type: protein-coding
Description: Rho GTPase activating protein 35
Entrez Gene ID: 2909
Genome: hg19
Position: chr19:47,364,254-47,508,334
Genome: hg38
Position: chr19:46,860,997-47,005,077
MIM: 605277 OMIM
HGNC: HGNC:4591 HGNC
Ensembl: ENSG00000160007 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Pathogenic	0	8
Likely pathogenic	0	18
Benign	0	6
Likely benign	0	6
not provided	21	0
Uncertain significance	0	110

Ranking

	ClinVar
	0
	0
	0
	146
	2

Frequency

EXAC_EAS

EXAC_EAS

HGVD

HGVD

TOMMO

TOMMO

Gene

Position

EXAC_EAS

EXAC_EAS

HGVD

HGVD

TOMMO

TOMMO

Gene

Position

Disease area statistics

Locus Zoom

Variants

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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

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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	GRF-1
SYNONYM	GRLF1
SYNONYM	P190-A
SYNONYM	P190A
SYNONYM	p190ARhoGAP
SYNONYM	p190RhoGAP
MIM	605277 OMIM
HGNC	HGNC:4591 HGNC
Ensembl	ENSG00000160007 Ensembl
AllianceGenome	HGNC:4591

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000672722.1	hg38	chr19	46,860,997	47,005,077	144,081
ENST00000672722.1	hg19	chr19	47,364,254	47,508,334	144,081

Key	Value
strand	+
UniProt	TSG
start	47,421,932
Gene Symbol	ARHGAP35
Entrez GeneId	2,909
Chr Band	19q13.3
end	47,508,332
chr	chr19

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