MAGEC3 MAGE family member C3

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: MAGEC3
Type: protein-coding
Description: MAGE family member C3
Entrez Gene ID: 139081
Genome: hg19
Position: chrX:140,926,102-140,985,618
Genome: hg38
Position: chrX:141,838,316-141,897,832
MIM: 300469 OMIM
HGNC: HGNC:23798 HGNC
Ensembl: ENSG00000165509 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	4
Likely benign	0	14
not provided	6	0
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

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
Category	:
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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	CT7.2
SYNONYM	HCA2
SYNONYM	MAGE-C3
SYNONYM	MAGEC4
MIM	300469 OMIM
HGNC	HGNC:23798 HGNC
Ensembl	ENSG00000165509 Ensembl
AllianceGenome	HGNC:23798

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000409007.1	hg38	chrX	141,896,235	141,897,832	1,598
ENST00000298296.1	hg38	chrX	141,838,316	141,897,832	59,517
ENST00000544766.5	hg38	chrX	141,894,666	141,897,832	3,167
ENST00000443323.2	hg38	chrX	141,880,562	141,897,832	17,271
ENST00000298296.1	hg19	chrX	140,926,102	140,985,618	59,517
ENST00000443323.2	hg19	chrX	140,968,348	140,985,618	17,271
ENST00000544766.5	hg19	chrX	140,982,452	140,985,618	3,167
ENST00000409007.1	hg19	chrX	140,984,021	140,985,618	1,598

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