COQ10B coenzyme Q10B
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 18 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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22 |
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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
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 | |||||
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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 |
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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MIM | 620737 OMIM |
HGNC | HGNC:25819 HGNC |
Ensembl | ENSG00000115520 Ensembl |
AllianceGenome | HGNC:25819 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000263960.7 | hg38 | chr2 | 197,453,552 | 197,475,310 | 21,759 |
ENST00000409010.1 | hg38 | chr2 | 197,453,794 | 197,474,410 | 20,617 |
ENST00000409398.5 | hg38 | chr2 | 197,453,493 | 197,474,168 | 20,676 |
ENST00000409398.5 | hg19 | chr2 | 198,318,217 | 198,338,892 | 20,676 |
ENST00000263960.7 | hg19 | chr2 | 198,318,276 | 198,340,034 | 21,759 |
ENST00000409010.1 | hg19 | chr2 | 198,318,518 | 198,339,134 | 20,617 |
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