RASSF1 Ras association domain family member 1

Go to:

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

Information

Symbol: RASSF1
Type: protein-coding
Description: Ras association domain family member 1
Entrez Gene ID: 11186
Genome: hg19
Position: chr3:50,367,219-50,378,272
Genome: hg38
Position: chr3:50,329,788-50,340,841
MIM: 605082 OMIM
HGNC: HGNC:9882 HGNC
Ensembl: ENSG00000068028 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	4
Likely benign	0	2
Uncertain significance	0	30

Ranking

	ClinVar
	0
	0
	0
	36
	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	123F2
SYNONYM	NORE2A
SYNONYM	RASSF1A
SYNONYM	RDA32
SYNONYM	REH3P21
MIM	605082 OMIM
HGNC	HGNC:9882 HGNC
Ensembl	ENSG00000068028 Ensembl
AllianceGenome	HGNC:9882

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000357043.6	hg38	chr3	50,329,788	50,340,841	11,054
ENST00000327761.7	hg38	chr3	50,329,782	50,337,464	7,683
ENST00000359365.9	hg38	chr3	50,329,788	50,340,836	11,049
ENST00000616212.4	hg38	chr3	50,329,786	50,340,936	11,151
ENST00000395126.7	hg38	chr3	50,329,788	50,338,233	8,446
ENST00000327761.7	hg19	chr3	50,367,213	50,374,895	7,683
ENST00000616212.4	hg19	chr3	50,367,217	50,378,367	11,151
ENST00000395126.7	hg19	chr3	50,367,219	50,375,664	8,446
ENST00000359365.9	hg19	chr3	50,367,219	50,378,267	11,049
ENST00000357043.6	hg19	chr3	50,367,219	50,378,272	11,054

Key	Value
strand	-
UniProt	TSG
start	50,367,216
Gene Symbol	RASSF1
Entrez GeneId	11,186
Chr Band	3p21.3
end	50,378,366
chr	chr3

Genome browser