ATP5MF ATP synthase membrane subunit f

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: ATP5MF
Type: protein-coding
Description: ATP synthase membrane subunit f
Entrez Gene ID: 9551
Genome: hg19
Position: chr7:99,055,818-99,063,790
Genome: hg38
Position: chr7:99,458,195-99,466,167
MIM: 619792 OMIM
HGNC: HGNC:848 HGNC
Ensembl: ENSG00000241468 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Uncertain significance	0	6

Ranking

	ClinVar
	0
	0
	0
	6
	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

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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

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
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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	ATP5J2
SYNONYM	ATP5JL
MIM	619792 OMIM
HGNC	HGNC:848 HGNC
Ensembl	ENSG00000241468 Ensembl
AllianceGenome	HGNC:848

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000359832.8	hg38	chr7	99,458,195	99,466,164	7,970
ENST00000449683.5	hg38	chr7	99,458,190	99,466,167	7,978
ENST00000394186.3	hg38	chr7	99,458,309	99,466,161	7,853
ENST00000488775.5	hg38	chr7	99,458,197	99,466,167	7,971
ENST00000292475.8	hg38	chr7	99,458,195	99,466,167	7,973
ENST00000449683.5	hg19	chr7	99,055,813	99,063,790	7,978
ENST00000359832.8	hg19	chr7	99,055,818	99,063,787	7,970
ENST00000292475.8	hg19	chr7	99,055,818	99,063,790	7,973
ENST00000488775.5	hg19	chr7	99,055,820	99,063,790	7,971
ENST00000394186.3	hg19	chr7	99,055,932	99,063,784	7,853

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