TRIM17 tripartite motif containing 17

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: TRIM17
Type: protein-coding
Description: tripartite motif containing 17
Entrez Gene ID: 51127
Genome: hg19
Position: chr1:228,595,641-228,603,730
Genome: hg38
Position: chr1:228,407,940-228,416,029
MIM: 606123 OMIM
HGNC: HGNC:13430 HGNC
Ensembl: ENSG00000162931 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	10
Likely benign	0	12
Uncertain significance	0	44

Ranking

	ClinVar
	0
	0
	0
	66
	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
Category	:
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Filtering	:

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	RBCC
SYNONYM	RNF16
SYNONYM	terf
MIM	606123 OMIM
HGNC	HGNC:13430 HGNC
Ensembl	ENSG00000162931 Ensembl
AllianceGenome	HGNC:13430

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000295033.7	hg38	chr1	228,408,036	228,416,664	8,629
ENST00000456946.6	hg38	chr1	228,408,700	228,416,757	8,058
ENST00000366698.7	hg38	chr1	228,407,935	228,416,861	8,927
ENST00000366697.6	hg38	chr1	228,407,940	228,416,029	8,090
ENST00000366698.7	hg19	chr1	228,595,636	228,604,562	8,927
ENST00000366697.6	hg19	chr1	228,595,641	228,603,730	8,090
ENST00000295033.7	hg19	chr1	228,595,737	228,604,365	8,629
ENST00000456946.6	hg19	chr1	228,596,401	228,604,458	8,058

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