CCL7 C-C motif chemokine ligand 7
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 16 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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16 |
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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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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 | FIC |
SYNONYM | MARC |
SYNONYM | MCP-3 |
SYNONYM | MCP3 |
SYNONYM | NC28 |
SYNONYM | SCYA6 |
SYNONYM | SCYA7 |
MIM | 158106 OMIM |
HGNC | HGNC:10634 HGNC |
Ensembl | ENSG00000108688 Ensembl |
AllianceGenome | HGNC:10634 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000394627.5 | hg38 | chr17 | 34,270,224 | 34,272,078 | 1,855 |
ENST00000394630.3 | hg38 | chr17 | 34,270,224 | 34,272,240 | 2,017 |
ENST00000378569.2 | hg38 | chr17 | 34,270,221 | 34,272,242 | 2,022 |
ENST00000378569.2 | hg19 | chr17 | 32,597,240 | 32,599,261 | 2,022 |
ENST00000394627.5 | hg19 | chr17 | 32,597,243 | 32,599,097 | 1,855 |
ENST00000394630.3 | hg19 | chr17 | 32,597,243 | 32,599,259 | 2,017 |
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