IRF7 interferon regulatory factor 7
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Pathogenic | 0 | 2 |
| Benign | 0 | 58 |
| Likely benign | 0 | 442 |
| Conflicting classifications of pathogenicity | 0 | 8 |
| Uncertain significance | 0 | 688 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
104 |
 |
1,078 |
 |
2 |
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | IMD39 |
| SYNONYM | IRF-7 |
| SYNONYM | IRF-7H |
| SYNONYM | IRF7A |
| SYNONYM | IRF7B |
| SYNONYM | IRF7C |
| SYNONYM | IRF7H |
| MIM | 605047 OMIM |
| HGNC | HGNC:6122 HGNC |
| Ensembl | ENSG00000185507 Ensembl |
| AllianceGenome | HGNC:6122 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000330243.9 | hg38 | chr11 | 612,591 | 615,970 | 3,380 |
| ENST00000348655.11 | hg38 | chr11 | 612,555 | 615,921 | 3,367 |
| ENST00000525445.6 | hg38 | chr11 | 612,555 | 615,950 | 3,396 |
| ENST00000397570.5 | hg38 | chr11 | 612,576 | 615,728 | 3,153 |
| ENST00000397566.5 | hg38 | chr11 | 612,555 | 615,728 | 3,174 |
| ENST00000397566.5 | hg19 | chr11 | 612,555 | 615,728 | 3,174 |
| ENST00000330243.9 | hg19 | chr11 | 612,591 | 615,970 | 3,380 |
| ENST00000348655.11 | hg19 | chr11 | 612,555 | 615,921 | 3,367 |
| ENST00000525445.6 | hg19 | chr11 | 612,555 | 615,950 | 3,396 |
| ENST00000397570.5 | hg19 | chr11 | 612,576 | 615,728 | 3,153 |
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