CXCL11 C-X-C motif chemokine ligand 11
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 10 |
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
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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 |
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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 |
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SYNONYM | H174 |
SYNONYM | I-TAC |
SYNONYM | IP-9 |
SYNONYM | IP9 |
SYNONYM | SCYB11 |
SYNONYM | SCYB9B |
SYNONYM | b-R1 |
MIM | 604852 OMIM |
HGNC | HGNC:10638 HGNC |
Ensembl | ENSG00000169248 Ensembl |
AllianceGenome | HGNC:10638 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000503860.1 | hg38 | chr4 | 76,034,690 | 76,041,415 | 6,726 |
ENST00000306621.8 | hg38 | chr4 | 76,033,682 | 76,036,070 | 2,389 |
ENST00000306621.8 | hg19 | chr4 | 76,954,835 | 76,957,223 | 2,389 |
ENST00000503860.1 | hg19 | chr4 | 76,955,843 | 76,962,568 | 6,726 |
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