TDRD3 tudor domain containing 3

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Variants
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Information

Symbol: TDRD3
Type: protein-coding
Description: tudor domain containing 3
Entrez Gene ID: 81550
Genome: hg19
Position: chr13:60,971,354-61,148,005
Genome: hg38
Position: chr13:60,397,220-60,573,871
MIM: 614392 OMIM
HGNC: HGNC:20612 HGNC
Ensembl: ENSG00000083544 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Likely benign	0	2
Uncertain significance	0	52

Ranking

	ClinVar
	0
	0
	0
	54
	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
Category	:
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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	:
Search word	:
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
MIM	614392 OMIM
HGNC	HGNC:20612 HGNC
Ensembl	ENSG00000083544 Ensembl
AllianceGenome	HGNC:20612

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000377881.8	hg38	chr13	60,397,220	60,573,871	176,652
ENST00000648252.1	hg38	chr13	60,397,831	60,573,864	176,034
ENST00000377894.6	hg38	chr13	60,396,988	60,573,877	176,890
ENST00000621840.4	hg38	chr13	60,434,047	60,573,870	139,824
ENST00000196169.7	hg38	chr13	60,396,457	60,573,878	177,422
ENST00000196169.7	hg19	chr13	60,970,591	61,148,012	177,422
ENST00000377894.6	hg19	chr13	60,971,122	61,148,011	176,890
ENST00000377881.8	hg19	chr13	60,971,354	61,148,005	176,652
ENST00000648252.1	hg19	chr13	60,971,965	61,147,998	176,034
ENST00000621840.4	hg19	chr13	61,008,181	61,148,004	139,824

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