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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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 | |||
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Entry | Origin | Type | Annotation |
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Target data | : |
MGeND data only
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Category | : |
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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 | 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 |
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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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