IRF3 interferon regulatory factor 3
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 12 |
Likely benign | 0 | 26 |
risk factor | 0 | 4 |
Uncertain significance | 0 | 70 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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6 |
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100 |
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4 |
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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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 | IIAE7 |
MIM | 603734 OMIM |
HGNC | HGNC:6118 HGNC |
Ensembl | ENSG00000126456 Ensembl |
AllianceGenome | HGNC:6118 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000601291.5 | hg38 | chr19 | 49,659,572 | 49,665,802 | 6,231 |
ENST00000596822.5 | hg38 | chr19 | 49,659,572 | 49,665,755 | 6,184 |
ENST00000593922.5 | hg38 | chr19 | 49,659,579 | 49,665,705 | 6,127 |
ENST00000377135.8 | hg38 | chr19 | 49,659,570 | 49,665,875 | 6,306 |
ENST00000377139.8 | hg38 | chr19 | 49,659,572 | 49,665,857 | 6,286 |
ENST00000596765.5 | hg38 | chr19 | 49,659,579 | 49,665,705 | 6,127 |
ENST00000600022.5 | hg38 | chr19 | 49,659,579 | 49,665,705 | 6,127 |
ENST00000599144.5 | hg38 | chr19 | 49,659,579 | 49,665,731 | 6,153 |
ENST00000598808.5 | hg38 | chr19 | 49,659,632 | 49,665,842 | 6,211 |
ENST00000309877.11 | hg38 | chr19 | 49,659,572 | 49,665,169 | 5,598 |
ENST00000599223.5 | hg38 | chr19 | 49,659,579 | 49,665,705 | 6,127 |
ENST00000597198.5 | hg38 | chr19 | 49,659,573 | 49,665,857 | 6,285 |
ENST00000442265.2 | hg38 | chr19 | 49,662,539 | 49,664,838 | 2,300 |
ENST00000600911.5 | hg38 | chr19 | 49,659,572 | 49,665,231 | 5,660 |
ENST00000377135.8 | hg19 | chr19 | 50,162,827 | 50,169,132 | 6,306 |
ENST00000309877.11 | hg19 | chr19 | 50,162,829 | 50,168,426 | 5,598 |
ENST00000377139.8 | hg19 | chr19 | 50,162,829 | 50,169,114 | 6,286 |
ENST00000442265.2 | hg19 | chr19 | 50,165,796 | 50,168,095 | 2,300 |
ENST00000596765.5 | hg19 | chr19 | 50,162,836 | 50,168,962 | 6,127 |
ENST00000593922.5 | hg19 | chr19 | 50,162,836 | 50,168,962 | 6,127 |
ENST00000596822.5 | hg19 | chr19 | 50,162,829 | 50,169,012 | 6,184 |
ENST00000597198.5 | hg19 | chr19 | 50,162,830 | 50,169,114 | 6,285 |
ENST00000598808.5 | hg19 | chr19 | 50,162,889 | 50,169,099 | 6,211 |
ENST00000599144.5 | hg19 | chr19 | 50,162,836 | 50,168,988 | 6,153 |
ENST00000600022.5 | hg19 | chr19 | 50,162,836 | 50,168,962 | 6,127 |
ENST00000599223.5 | hg19 | chr19 | 50,162,836 | 50,168,962 | 6,127 |
ENST00000600911.5 | hg19 | chr19 | 50,162,829 | 50,168,488 | 5,660 |
ENST00000601291.5 | hg19 | chr19 | 50,162,829 | 50,169,059 | 6,231 |
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