CCR8 C-C motif chemokine receptor 8
Clinical Significance
MGeND | ClinVar | |
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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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32 |
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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-8 |
SYNONYM | CCR-8 |
SYNONYM | CDw198 |
SYNONYM | CKRL1 |
SYNONYM | CMKBR8 |
SYNONYM | CMKBRL2 |
SYNONYM | CY6 |
SYNONYM | GPRCY6 |
SYNONYM | TER1 |
MIM | 601834 OMIM |
HGNC | HGNC:1609 HGNC |
Ensembl | ENSG00000179934 Ensembl |
AllianceGenome | HGNC:1609 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000326306.5 | hg38 | chr3 | 39,329,709 | 39,333,680 | 3,972 |
ENST00000414803.1 | hg38 | chr3 | 39,329,773 | 39,333,511 | 3,739 |
ENST00000326306.5 | hg19 | chr3 | 39,371,200 | 39,375,171 | 3,972 |
ENST00000414803.1 | hg19 | chr3 | 39,371,264 | 39,375,002 | 3,739 |
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