IL33 interleukin 33
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 12 |
Likely benign | 0 | 2 |
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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40 |
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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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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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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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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 | C9orf26 |
SYNONYM | DVS27 |
SYNONYM | IL1F11 |
SYNONYM | NF-HEV |
SYNONYM | NFEHEV |
MIM | 608678 OMIM |
HGNC | HGNC:16028 HGNC |
Ensembl | ENSG00000137033 Ensembl |
AllianceGenome | HGNC:16028 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000381434.7 | hg38 | chr9 | 6,241,682 | 6,257,983 | 16,302 |
ENST00000417746.6 | hg38 | chr9 | 6,215,786 | 6,257,982 | 42,197 |
ENST00000611532.4 | hg38 | chr9 | 6,241,680 | 6,256,223 | 14,544 |
ENST00000456383.3 | hg38 | chr9 | 6,241,695 | 6,257,982 | 16,288 |
ENST00000682010.1 | hg38 | chr9 | 6,215,807 | 6,257,983 | 42,177 |
ENST00000417746.6 | hg19 | chr9 | 6,215,786 | 6,257,982 | 42,197 |
ENST00000682010.1 | hg19 | chr9 | 6,215,807 | 6,257,983 | 42,177 |
ENST00000611532.4 | hg19 | chr9 | 6,241,680 | 6,256,223 | 14,544 |
ENST00000381434.7 | hg19 | chr9 | 6,241,682 | 6,257,983 | 16,302 |
ENST00000456383.3 | hg19 | chr9 | 6,241,695 | 6,257,982 | 16,288 |
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