AOC3 amine oxidase copper containing 3

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: AOC3
Type: protein-coding
Description: amine oxidase copper containing 3
Entrez Gene ID: 8639
Genome: hg19
Position: chr17:41,003,216-41,010,141
Genome: hg38
Position: chr17:42,851,199-42,858,124
MIM: 603735 OMIM
HGNC: HGNC:550 HGNC
Ensembl: ENSG00000131471 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	12
Likely benign	0	20
Uncertain significance	0	88

Ranking

	ClinVar
	0
	0
	2
	116
	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
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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	HPAO
SYNONYM	SSAO
SYNONYM	VAP-1
SYNONYM	VAP1
MIM	603735 OMIM
HGNC	HGNC:550 HGNC
Ensembl	ENSG00000131471 Ensembl
AllianceGenome	HGNC:550

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000591562.1	hg38	chr17	42,854,078	42,858,130	4,053
ENST00000613571.1	hg38	chr17	42,851,184	42,858,128	6,945
ENST00000617500.4	hg38	chr17	42,853,243	42,858,128	4,886
ENST00000308423.7	hg38	chr17	42,851,199	42,858,124	6,926
ENST00000613571.1	hg19	chr17	41,003,201	41,010,145	6,945
ENST00000308423.7	hg19	chr17	41,003,216	41,010,141	6,926
ENST00000617500.4	hg19	chr17	41,005,260	41,010,145	4,886
ENST00000591562.1	hg19	chr17	41,006,095	41,010,147	4,053

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