FBXO3 F-box protein 3
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 4 |
not provided | 1 | 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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34 |
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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
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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Target data | : |
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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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 | FBA |
SYNONYM | FBX3 |
MIM | 609089 OMIM |
HGNC | HGNC:13582 HGNC |
Ensembl | ENSG00000110429 Ensembl |
AllianceGenome | HGNC:13582 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000532057.5 | hg38 | chr11 | 33,741,739 | 33,753,399 | 11,661 |
ENST00000531080.5 | hg38 | chr11 | 33,741,442 | 33,753,400 | 11,959 |
ENST00000530401.5 | hg38 | chr11 | 33,740,965 | 33,774,518 | 33,554 |
ENST00000526785.5 | hg38 | chr11 | 33,740,939 | 33,774,347 | 33,409 |
ENST00000534136.5 | hg38 | chr11 | 33,744,685 | 33,774,504 | 29,820 |
ENST00000448981.6 | hg38 | chr11 | 33,746,743 | 33,774,543 | 27,801 |
ENST00000265651.8 | hg38 | chr11 | 33,740,944 | 33,774,520 | 33,577 |
ENST00000526785.5 | hg19 | chr11 | 33,762,485 | 33,795,893 | 33,409 |
ENST00000265651.8 | hg19 | chr11 | 33,762,490 | 33,796,066 | 33,577 |
ENST00000530401.5 | hg19 | chr11 | 33,762,511 | 33,796,064 | 33,554 |
ENST00000531080.5 | hg19 | chr11 | 33,762,988 | 33,774,946 | 11,959 |
ENST00000532057.5 | hg19 | chr11 | 33,763,285 | 33,774,945 | 11,661 |
ENST00000534136.5 | hg19 | chr11 | 33,766,231 | 33,796,050 | 29,820 |
ENST00000448981.6 | hg19 | chr11 | 33,768,289 | 33,796,089 | 27,801 |
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