CXCL8 C-X-C motif chemokine ligand 8
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 6 |
| Uncertain significance | 0 | 4 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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10 |
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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
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 | |||||||||||
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | GCP-1 |
| SYNONYM | GCP1 |
| SYNONYM | IL8 |
| SYNONYM | LECT |
| SYNONYM | LUCT |
| SYNONYM | LYNAP |
| SYNONYM | MDNCF |
| SYNONYM | MONAP |
| SYNONYM | NAF |
| SYNONYM | NAP-1 |
| SYNONYM | NAP1 |
| SYNONYM | SCYB8 |
| MIM | 146930 OMIM |
| HGNC | HGNC:6025 HGNC |
| Ensembl | ENSG00000169429 Ensembl |
| AllianceGenome | HGNC:6025 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000401931.1 | hg38 | chr4 | 73,740,541 | 73,742,330 | 1,790 |
| ENST00000307407.8 | hg38 | chr4 | 73,740,569 | 73,743,716 | 3,148 |
| ENST00000401931.1 | hg19 | chr4 | 74,606,258 | 74,608,047 | 1,790 |
| ENST00000307407.8 | hg19 | chr4 | 74,606,286 | 74,609,433 | 3,148 |
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