COQ4 coenzyme Q4
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 12 | 52 |
Likely pathogenic | 2 | 28 |
Benign | 0 | 36 |
Likely benign | 0 | 250 |
Conflicting classifications of pathogenicity | 0 | 22 |
Uncertain significance | 0 | 184 |
Ranking
ClinVar | |
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0 |
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0 |
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90 |
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428 |
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16 |
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
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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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SYNONYM | CGI-92 |
SYNONYM | COQ10D7 |
SYNONYM | SPAX10 |
MIM | 612898 OMIM |
HGNC | HGNC:19693 HGNC |
Ensembl | ENSG00000167113 Ensembl |
AllianceGenome | HGNC:19693 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000372875.3 | hg38 | chr9 | 128,322,852 | 128,326,400 | 3,549 |
ENST00000300452.8 | hg38 | chr9 | 128,322,839 | 128,334,072 | 11,234 |
ENST00000608951.5 | hg38 | chr9 | 128,322,582 | 128,323,584 | 1,003 |
ENST00000609948.1 | hg38 | chr9 | 128,322,544 | 128,323,586 | 1,043 |
ENST00000609948.1 | hg19 | chr9 | 131,084,823 | 131,085,865 | 1,043 |
ENST00000608951.5 | hg19 | chr9 | 131,084,861 | 131,085,863 | 1,003 |
ENST00000300452.8 | hg19 | chr9 | 131,085,118 | 131,096,351 | 11,234 |
ENST00000372875.3 | hg19 | chr9 | 131,085,131 | 131,088,679 | 3,549 |
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