MED6 mediator complex subunit 6

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Variants
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Information

Symbol: MED6
Type: protein-coding
Description: mediator complex subunit 6
Entrez Gene ID: 10001
Genome: hg19
Position: chr14:71,049,938-71,067,407
Genome: hg38
Position: chr14:70,583,221-70,600,690
MIM: 602984 OMIM
HGNC: HGNC:19970 HGNC
Ensembl: ENSG00000133997 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Uncertain significance	0	8

Ranking

	ClinVar
	0
	0
	0
	8
	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
SYNONYM	ARC33
SYNONYM	NY-REN-28
MIM	602984 OMIM
HGNC	HGNC:19970 HGNC
Ensembl	ENSG00000133997 Ensembl
AllianceGenome	HGNC:19970

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000256379.10	hg38	chr14	70,583,221	70,600,655	17,435
ENST00000615788.4	hg38	chr14	70,583,221	70,600,690	17,470
ENST00000430055.6	hg38	chr14	70,584,086	70,600,655	16,570
ENST00000554963.5	hg38	chr14	70,581,257	70,600,643	19,387
ENST00000440435.2	hg38	chr14	70,584,525	70,600,655	16,131
ENST00000554963.5	hg19	chr14	71,047,974	71,067,360	19,387
ENST00000256379.10	hg19	chr14	71,049,938	71,067,372	17,435
ENST00000615788.4	hg19	chr14	71,049,938	71,067,407	17,470
ENST00000430055.6	hg19	chr14	71,050,803	71,067,372	16,570
ENST00000440435.2	hg19	chr14	71,051,242	71,067,372	16,131

Key	Value
strand	-
start	71,049,937
Gene Symbol	MED6
Entrez GeneId	10,001
Chr Band	14q24.2
end	71,067,406
chr	chr14

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