RRAS2 RAS related 2

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: RRAS2
Type: protein-coding
Description: RAS related 2
Entrez Gene ID: 22800
Genome: hg19
Position: chr11:14,299,468-14,380,729
Genome: hg38
Position: chr11:14,277,922-14,359,183
MIM: 600098 OMIM
HGNC: HGNC:17271 HGNC
Ensembl: ENSG00000133818 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Pathogenic	0	12
Likely pathogenic	0	8
Benign	0	24
Likely benign	0	26
Conflicting classifications of pathogenicity	0	4
Uncertain significance	0	66

Ranking

	ClinVar
	0
	0
	24
	108
	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

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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

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	NS12
SYNONYM	TC21
MIM	600098 OMIM
HGNC	HGNC:17271 HGNC
Ensembl	ENSG00000133818 Ensembl
AllianceGenome	HGNC:17271

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000534746.5	hg38	chr11	14,278,939	14,354,500	75,562
ENST00000537760.5	hg38	chr11	14,277,926	14,364,506	86,581
ENST00000256196.9	hg38	chr11	14,277,922	14,359,183	81,262
ENST00000526063.5	hg38	chr11	14,279,103	14,358,485	79,383
ENST00000414023.6	hg38	chr11	14,277,964	14,295,859	17,896
ENST00000532814.5	hg38	chr11	14,279,110	14,358,485	79,376
ENST00000529237.5	hg38	chr11	14,278,682	14,364,506	85,825
ENST00000256196.9	hg19	chr11	14,299,468	14,380,729	81,262
ENST00000537760.5	hg19	chr11	14,299,472	14,386,052	86,581
ENST00000414023.6	hg19	chr11	14,299,510	14,317,405	17,896
ENST00000529237.5	hg19	chr11	14,300,228	14,386,052	85,825
ENST00000534746.5	hg19	chr11	14,300,485	14,376,046	75,562
ENST00000526063.5	hg19	chr11	14,300,649	14,380,031	79,383
ENST00000532814.5	hg19	chr11	14,300,656	14,380,031	79,376

Key	Value
strand	-
UniProt	OG
start	14,299,465
Gene Symbol	RRAS2
Entrez GeneId	22,800
Chr Band	11p15.2
end	14,386,051
chr	chr11

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