CYBRD1 cytochrome b reductase 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 6 |
Uncertain significance | 0 | 30 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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38 |
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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
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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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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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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 | CYB561A2 |
SYNONYM | DCYTB |
SYNONYM | FRRS3 |
MIM | 605745 OMIM |
HGNC | HGNC:20797 HGNC |
Ensembl | ENSG00000071967 Ensembl |
AllianceGenome | HGNC:20797 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000409484.5 | hg38 | chr2 | 171,522,247 | 171,555,607 | 33,361 |
ENST00000321348.9 | hg38 | chr2 | 171,522,474 | 171,558,129 | 35,656 |
ENST00000375252.3 | hg38 | chr2 | 171,522,477 | 171,557,646 | 35,170 |
ENST00000409484.5 | hg19 | chr2 | 172,378,757 | 172,412,117 | 33,361 |
ENST00000321348.9 | hg19 | chr2 | 172,378,984 | 172,414,639 | 35,656 |
ENST00000375252.3 | hg19 | chr2 | 172,378,987 | 172,414,156 | 35,170 |
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