MYO3B myosin IIIB
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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MIM | 610040 OMIM |
HGNC | HGNC:15576 HGNC |
Ensembl | ENSG00000071909 Ensembl |
AllianceGenome | HGNC:15576 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000408978.9 | hg38 | chr2 | 170,178,147 | 170,655,167 | 477,021 |
ENST00000409044.7 | hg38 | chr2 | 170,178,145 | 170,654,481 | 476,337 |
ENST00000409044.7 | hg19 | chr2 | 171,034,655 | 171,510,991 | 476,337 |
ENST00000408978.9 | hg19 | chr2 | 171,034,657 | 171,511,677 | 477,021 |
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