NFKBIB NFKB inhibitor beta
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 6 |
Uncertain significance | 0 | 34 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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40 |
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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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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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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 | IKBB |
SYNONYM | TRIP9 |
MIM | 604495 OMIM |
HGNC | HGNC:7798 HGNC |
Ensembl | ENSG00000104825 Ensembl |
AllianceGenome | HGNC:7798 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000392079.7 | hg38 | chr19 | 38,899,700 | 38,908,891 | 9,192 |
ENST00000572515.5 | hg38 | chr19 | 38,899,952 | 38,908,538 | 8,587 |
ENST00000313582.6 | hg38 | chr19 | 38,899,969 | 38,908,889 | 8,921 |
ENST00000392079.7 | hg19 | chr19 | 39,390,340 | 39,399,531 | 9,192 |
ENST00000572515.5 | hg19 | chr19 | 39,390,592 | 39,399,178 | 8,587 |
ENST00000313582.6 | hg19 | chr19 | 39,390,609 | 39,399,529 | 8,921 |
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