MYO9B myosin IXB

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: MYO9B
Type: protein-coding
Description: myosin IXB
Entrez Gene ID: 4650
Genome: hg19
Position: chr19:17,186,587-17,324,095
Genome: hg38
Position: chr19:17,075,777-17,213,286
MIM: 602129 OMIM
HGNC: HGNC:7609 HGNC
Ensembl: ENSG00000099331 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	32
Likely benign	0	96
Conflicting classifications of pathogenicity	0	4
Uncertain significance	0	250

Ranking

	ClinVar
	0
	0
	8
	362
	6

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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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

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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	CELIAC4
SYNONYM	MYR5
MIM	602129 OMIM
HGNC	HGNC:7609 HGNC
Ensembl	ENSG00000099331 Ensembl
AllianceGenome	HGNC:7609

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000397274.6	hg38	chr19	17,101,656	17,213,294	111,639
ENST00000595618.5	hg38	chr19	17,075,781	17,213,295	137,515
ENST00000594824.5	hg38	chr19	17,075,786	17,213,284	137,499
ENST00000682292.1	hg38	chr19	17,075,777	17,213,286	137,510
ENST00000595618.5	hg19	chr19	17,186,591	17,324,104	137,514
ENST00000594824.5	hg19	chr19	17,186,596	17,324,093	137,498
ENST00000397274.6	hg19	chr19	17,212,466	17,324,103	111,638
ENST00000682292.1	hg19	chr19	17,186,587	17,324,095	137,509

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