IL22 interleukin 22
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 22 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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26 |
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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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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
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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 | IL-21 |
SYNONYM | IL-22 |
SYNONYM | IL-D110 |
SYNONYM | IL-TIF |
SYNONYM | ILTIF |
SYNONYM | TIFIL-23 |
SYNONYM | TIFa |
SYNONYM | zcyto18 |
MIM | 605330 OMIM |
HGNC | HGNC:14900 HGNC |
Ensembl | ENSG00000127318 Ensembl |
AllianceGenome | HGNC:14900 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000328087.6 | hg38 | chr12 | 68,248,789 | 68,253,502 | 4,714 |
ENST00000538666.6 | hg38 | chr12 | 68,248,242 | 68,253,604 | 5,363 |
ENST00000538666.6 | hg19 | chr12 | 68,642,022 | 68,647,384 | 5,363 |
ENST00000328087.6 | hg19 | chr12 | 68,642,569 | 68,647,282 | 4,714 |
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