VAMP2 vesicle associated membrane protein 2

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: VAMP2
Type: protein-coding
Description: vesicle associated membrane protein 2
Entrez Gene ID: 6844
Genome: hg19
Position: chr17:8,064,137-8,066,250
Genome: hg38
Position: chr17:8,160,819-8,162,932
MIM: 185881 OMIM
HGNC: HGNC:12643 HGNC
Ensembl: ENSG00000220205 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Pathogenic	0	10
Likely pathogenic	0	8
Benign	0	2
Likely benign	0	10
Conflicting classifications of pathogenicity	0	2
Uncertain significance	0	24

Ranking

	ClinVar
	0
	0
	6
	42
	6

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

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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

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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	NEDHAHM
SYNONYM	SYB2
SYNONYM	VAMP-2
MIM	185881 OMIM
HGNC	HGNC:12643 HGNC
Ensembl	ENSG00000220205 Ensembl
AllianceGenome	HGNC:12643

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000488857.5	hg38	chr17	8,160,819	8,162,932	2,114
ENST00000404970.3	hg38	chr17	8,160,406	8,163,546	3,141
ENST00000481878.1	hg38	chr17	8,161,319	8,162,948	1,630
ENST00000316509.11	hg38	chr17	8,159,149	8,162,948	3,800
ENST00000316509.11	hg19	chr17	8,062,467	8,066,266	3,800
ENST00000404970.3	hg19	chr17	8,063,724	8,066,864	3,141
ENST00000488857.5	hg19	chr17	8,064,137	8,066,250	2,114
ENST00000481878.1	hg19	chr17	8,064,637	8,066,266	1,630

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