TRAF7 TNF receptor associated factor 7

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Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: TRAF7
Type: protein-coding
Description: TNF receptor associated factor 7
Entrez Gene ID: 84231
Genome: hg19
Position: chr16:2,205,783-2,228,130
Genome: hg38
Position: chr16:2,155,782-2,178,129
MIM: 606692 OMIM
HGNC: HGNC:20456 HGNC
Ensembl: ENSG00000131653 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Pathogenic	2	16
Likely pathogenic	0	14
Benign	0	16
Likely benign	0	74
Conflicting classifications of pathogenicity	0	8
not provided	16	0
Uncertain significance	0	112

Ranking

	ClinVar
	0
	0
	28
	190
	8

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

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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	CAFDADD
SYNONYM	RFWD1
SYNONYM	RNF119
MIM	606692 OMIM
HGNC	HGNC:20456 HGNC
Ensembl	ENSG00000131653 Ensembl
AllianceGenome	HGNC:20456

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000567653.5	hg38	chr16	2,155,804	2,168,510	12,707
ENST00000565383.5	hg38	chr16	2,155,698	2,168,515	12,818
ENST00000326181.11	hg38	chr16	2,155,782	2,178,129	22,348
ENST00000565383.5	hg19	chr16	2,205,699	2,218,516	12,818
ENST00000326181.11	hg19	chr16	2,205,783	2,228,130	22,348
ENST00000567653.5	hg19	chr16	2,205,805	2,218,511	12,707

Key	Value
strand	+
start	2,205,798
Vogelstein	TSG
Gene Symbol	TRAF7
Entrez GeneId	84,231
Chr Band	16p13.3
end	2,228,129
chr	chr16
Name	tumour necrosis factor receptor-associated factor 7

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