VCAM1 vascular cell adhesion molecule 1

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: VCAM1
Type: protein-coding
Description: vascular cell adhesion molecule 1
Entrez Gene ID: 7412
Genome: hg19
Position: chr1:101,185,298-101,204,601
Genome: hg38
Position: chr1:100,719,742-100,739,045
MIM: 192225 OMIM
HGNC: HGNC:12663 HGNC
Ensembl: ENSG00000162692 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	2
Likely benign	0	16
Uncertain significance	0	64

Ranking

	ClinVar
	0
	0
	0
	82
	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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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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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	CD106
SYNONYM	INCAM-100
MIM	192225 OMIM
HGNC	HGNC:12663 HGNC
Ensembl	ENSG00000162692 Ensembl
AllianceGenome	HGNC:12663

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000294728.7	hg38	chr1	100,719,742	100,739,045	19,304
ENST00000347652.6	hg38	chr1	100,719,755	100,739,045	19,291
ENST00000370115.1	hg38	chr1	100,719,764	100,739,038	19,275
ENST00000370119.8	hg38	chr1	100,719,742	100,738,613	18,872
ENST00000370119.8	hg19	chr1	101,185,298	101,204,169	18,872
ENST00000294728.7	hg19	chr1	101,185,298	101,204,601	19,304
ENST00000347652.6	hg19	chr1	101,185,311	101,204,601	19,291
ENST00000370115.1	hg19	chr1	101,185,320	101,204,594	19,275

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