CCR4 C-C motif chemokine receptor 4
Clinical Significance
MGeND | ClinVar | |
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Likely benign | 0 | 2 |
Uncertain significance | 0 | 32 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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34 |
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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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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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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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 | CC-CKR-4 |
SYNONYM | CD194 |
SYNONYM | CKR4 |
SYNONYM | CMKBR4 |
SYNONYM | ChemR13 |
SYNONYM | HGCN:14099 |
SYNONYM | K5-5 |
MIM | 604836 OMIM |
HGNC | HGNC:1605 HGNC |
Ensembl | ENSG00000183813 Ensembl |
AllianceGenome | HGNC:1605 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000330953.6 | hg38 | chr3 | 32,951,644 | 32,956,349 | 4,706 |
ENST00000330953.6 | hg19 | chr3 | 32,993,136 | 32,997,841 | 4,706 |
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