IL6 interleukin 6
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 10 |
| Likely benign | 0 | 6 |
| not provided | 141 | 0 |
| other; risk factor | 0 | 2 |
| Uncertain significance | 0 | 8 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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6 |
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16 |
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4 |
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
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 | BSF-2 |
| SYNONYM | BSF2 |
| SYNONYM | CDF |
| SYNONYM | HGF |
| SYNONYM | HSF |
| SYNONYM | IFN-beta-2 |
| SYNONYM | IFNB2 |
| SYNONYM | IL-6 |
| MIM | 147620 OMIM |
| HGNC | HGNC:6018 HGNC |
| Ensembl | ENSG00000136244 Ensembl |
| AllianceGenome | HGNC:6018 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000401651.5 | hg38 | chr7 | 22,727,147 | 22,729,803 | 2,657 |
| ENST00000485300.1 | hg38 | chr7 | 22,727,200 | 22,731,694 | 4,495 |
| ENST00000404625.5 | hg38 | chr7 | 22,725,884 | 22,732,002 | 6,119 |
| ENST00000406575.1 | hg38 | chr7 | 22,727,240 | 22,729,815 | 2,576 |
| ENST00000258743.10 | hg38 | chr7 | 22,727,200 | 22,731,998 | 4,799 |
| ENST00000401630.7 | hg38 | chr7 | 22,727,224 | 22,731,729 | 4,506 |
| ENST00000407492.5 | hg38 | chr7 | 22,727,214 | 22,732,002 | 4,789 |
| ENST00000404625.5 | hg19 | chr7 | 22,765,503 | 22,771,621 | 6,119 |
| ENST00000401651.5 | hg19 | chr7 | 22,766,766 | 22,769,422 | 2,657 |
| ENST00000485300.1 | hg19 | chr7 | 22,766,819 | 22,771,313 | 4,495 |
| ENST00000258743.10 | hg19 | chr7 | 22,766,819 | 22,771,617 | 4,799 |
| ENST00000407492.5 | hg19 | chr7 | 22,766,833 | 22,771,621 | 4,789 |
| ENST00000401630.7 | hg19 | chr7 | 22,766,843 | 22,771,348 | 4,506 |
| ENST00000406575.1 | hg19 | chr7 | 22,766,859 | 22,769,434 | 2,576 |
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