INO80E INO80 complex subunit E

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
Locus Zoom
Variants
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Information

Symbol: INO80E
Type: protein-coding
Description: INO80 complex subunit E
Entrez Gene ID: 283899
Genome: hg19
Position: chr16:30,007,562-30,017,112
Genome: hg38
Position: chr16:29,996,241-30,005,791
HGNC: HGNC:26905 HGNC
Ensembl: ENSG00000169592 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Likely benign	0	4
not provided	9	0
Uncertain significance	0	48

Ranking

	ClinVar
	0
	0
	0
	52
	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

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	CCDC95
HGNC	HGNC:26905 HGNC
Ensembl	ENSG00000169592 Ensembl
AllianceGenome	HGNC:26905

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000567705.5	hg38	chr16	29,996,250	30,005,577	9,328
ENST00000563197.6	hg38	chr16	29,996,241	30,005,791	9,551
ENST00000304516.11	hg38	chr16	29,995,715	30,005,717	10,003
ENST00000620599.4	hg38	chr16	29,996,210	30,001,229	5,020
ENST00000567254.5	hg38	chr16	29,996,244	30,001,575	5,332
ENST00000304516.11	hg19	chr16	30,007,036	30,017,038	10,003
ENST00000620599.4	hg19	chr16	30,007,531	30,012,550	5,020
ENST00000563197.6	hg19	chr16	30,007,562	30,017,112	9,551
ENST00000567254.5	hg19	chr16	30,007,565	30,012,896	5,332
ENST00000567705.5	hg19	chr16	30,007,571	30,016,898	9,328

Key	Value
strand	+
start	30,007,529
Gene Symbol	INO80E
Entrez GeneId	283,899
Chr Band	16p11.2
end	30,017,114
chr	chr16

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