IL21 interleukin 21
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 2 |
Benign | 0 | 16 |
Likely benign | 0 | 60 |
Conflicting classifications of pathogenicity | 0 | 2 |
Uncertain significance | 0 | 92 |
Ranking
ClinVar | |
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0 |
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0 |
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10 |
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158 |
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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 |
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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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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 | CVID11 |
SYNONYM | IL-21 |
SYNONYM | Za11 |
MIM | 605384 OMIM |
HGNC | HGNC:6005 HGNC |
Ensembl | ENSG00000138684 Ensembl |
AllianceGenome | HGNC:6005 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000611104.2 | hg38 | chr4 | 122,612,710 | 122,621,011 | 8,302 |
ENST00000648588.1 | hg38 | chr4 | 122,610,108 | 122,621,066 | 10,959 |
ENST00000648588.1 | hg19 | chr4 | 123,531,263 | 123,542,221 | 10,959 |
ENST00000611104.2 | hg19 | chr4 | 123,533,865 | 123,542,166 | 8,302 |
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