MYH10 myosin heavy chain 10
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Pathogenic | 0 | 6 |
| Likely pathogenic | 1 | 2 |
| Benign | 0 | 28 |
| Likely benign | 0 | 48 |
| Conflicting classifications of pathogenicity | 0 | 2 |
| Uncertain significance | 0 | 238 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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14 |
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294 |
![]() |
8 |
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| Filtering | : |
| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
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| Category | : |
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| Filtering | : |
| Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | NMMHC-IIB |
| SYNONYM | NMMHCB |
| MIM | 160776 OMIM |
| HGNC | HGNC:7568 HGNC |
| Ensembl | ENSG00000133026 Ensembl |
| AllianceGenome | HGNC:7568 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000693441.1 | hg38 | chr17 | 8,474,215 | 8,630,067 | 155,853 |
| ENST00000687178.1 | hg38 | chr17 | 8,474,215 | 8,631,343 | 157,129 |
| ENST00000692526.1 | hg38 | chr17 | 8,474,215 | 8,630,807 | 156,593 |
| ENST00000269243.8 | hg38 | chr17 | 8,474,212 | 8,630,761 | 156,550 |
| ENST00000379980.8 | hg38 | chr17 | 8,474,207 | 8,630,761 | 156,555 |
| ENST00000686654.1 | hg38 | chr17 | 8,474,215 | 8,629,776 | 155,562 |
| ENST00000688902.1 | hg38 | chr17 | 8,474,215 | 8,631,376 | 157,162 |
| ENST00000360416.8 | hg38 | chr17 | 8,474,224 | 8,630,725 | 156,502 |
| ENST00000684843.1 | hg38 | chr17 | 8,474,215 | 8,631,375 | 157,161 |
| ENST00000269243.8 | hg19 | chr17 | 8,377,530 | 8,534,079 | 156,550 |
| ENST00000360416.8 | hg19 | chr17 | 8,377,542 | 8,534,043 | 156,502 |
| ENST00000379980.8 | hg19 | chr17 | 8,377,525 | 8,534,079 | 156,555 |
| ENST00000684843.1 | hg19 | chr17 | 8,377,533 | 8,534,693 | 157,161 |
| ENST00000686654.1 | hg19 | chr17 | 8,377,533 | 8,533,094 | 155,562 |
| ENST00000687178.1 | hg19 | chr17 | 8,377,533 | 8,534,661 | 157,129 |
| ENST00000688902.1 | hg19 | chr17 | 8,377,533 | 8,534,694 | 157,162 |
| ENST00000692526.1 | hg19 | chr17 | 8,377,533 | 8,534,125 | 156,593 |
| ENST00000693441.1 | hg19 | chr17 | 8,377,533 | 8,533,385 | 155,853 |
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