IL10 interleukin 10
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 22 |
Likely benign | 0 | 100 |
Conflicting classifications of pathogenicity | 0 | 2 |
not provided | 2 | 0 |
Uncertain risk allele | 0 | 2 |
Uncertain significance | 0 | 96 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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10 |
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208 |
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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
Locus Zoom
Variants
Search Word
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 |
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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | CSIF |
SYNONYM | GVHDS |
SYNONYM | IL-10 |
SYNONYM | IL10A |
SYNONYM | TGIF |
MIM | 124092 OMIM |
HGNC | HGNC:5962 HGNC |
Ensembl | ENSG00000136634 Ensembl |
AllianceGenome | HGNC:5962 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000423557.1 | hg38 | chr1 | 206,767,602 | 206,772,494 | 4,893 |
ENST00000659642.2 | hg38 | chr1 | 206,768,110 | 206,774,538 | 6,429 |
ENST00000471071.2 | hg38 | chr1 | 206,768,110 | 206,771,199 | 3,090 |
ENST00000659065.2 | hg38 | chr1 | 206,768,110 | 206,774,541 | 6,432 |
ENST00000664374.2 | hg38 | chr1 | 206,768,110 | 206,774,541 | 6,432 |
ENST00000423557.1 | hg19 | chr1 | 206,940,947 | 206,945,839 | 4,893 |
ENST00000471071.2 | hg19 | chr1 | 206,941,455 | 206,944,544 | 3,090 |
ENST00000659642.2 | hg19 | chr1 | 206,941,455 | 206,947,883 | 6,429 |
ENST00000659065.2 | hg19 | chr1 | 206,941,455 | 206,947,886 | 6,432 |
ENST00000664374.2 | hg19 | chr1 | 206,941,455 | 206,947,886 | 6,432 |
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