FBXO9 F-box protein 9
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 4 | 0 |
Uncertain significance | 0 | 28 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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28 |
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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
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 |
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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 | FBX9 |
SYNONYM | NY-REN-57 |
SYNONYM | VCIA1 |
SYNONYM | dJ341E18.2 |
MIM | 609091 OMIM |
HGNC | HGNC:13588 HGNC |
Ensembl | ENSG00000112146 Ensembl |
AllianceGenome | HGNC:13588 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000244426.10 | hg38 | chr6 | 53,070,852 | 53,100,873 | 30,022 |
ENST00000370939.7 | hg38 | chr6 | 53,064,998 | 53,097,888 | 32,891 |
ENST00000323557.12 | hg38 | chr6 | 53,065,404 | 53,100,873 | 35,470 |
ENST00000370939.7 | hg19 | chr6 | 52,929,796 | 52,962,686 | 32,891 |
ENST00000323557.12 | hg19 | chr6 | 52,930,202 | 52,965,671 | 35,470 |
ENST00000244426.10 | hg19 | chr6 | 52,935,650 | 52,965,671 | 30,022 |
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