MOV10L1 Mov10 like RNA helicase 1

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

Symbol: MOV10L1
Type: protein-coding
Description: Mov10 like RNA helicase 1
Entrez Gene ID: 54456
Genome: hg19
Position: chr22:50,528,435-50,600,116
Genome: hg38
Position: chr22:50,090,006-50,161,687
MIM: 605794 OMIM
HGNC: HGNC:7201 HGNC
Ensembl: ENSG00000073146 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Pathogenic	0	4
Likely pathogenic	0	2
Benign	0	10
Likely benign	0	14
not provided	1	0
Uncertain significance	0	146

Ranking

	ClinVar
	0
	0
	0
	174
	2

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

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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

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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	CHAMP
SYNONYM	DJ402G11.8
SYNONYM	SPGF73
MIM	605794 OMIM
HGNC	HGNC:7201 HGNC
Ensembl	ENSG00000073146 Ensembl
AllianceGenome	HGNC:7201

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000540615.5	hg38	chr22	50,090,256	50,161,686	71,431
ENST00000354853.2	hg38	chr22	50,149,389	50,159,257	9,869
ENST00000262794.10	hg38	chr22	50,090,006	50,161,687	71,682
ENST00000395858.7	hg38	chr22	50,090,065	50,161,690	71,626
ENST00000395852.5	hg38	chr22	50,146,965	50,161,677	14,713
ENST00000262794.10	hg19	chr22	50,528,435	50,600,116	71,682
ENST00000395858.7	hg19	chr22	50,528,494	50,600,119	71,626
ENST00000540615.5	hg19	chr22	50,528,685	50,600,115	71,431
ENST00000395852.5	hg19	chr22	50,585,394	50,600,106	14,713
ENST00000354853.2	hg19	chr22	50,587,818	50,597,686	9,869

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