CCL26 C-C motif chemokine ligand 26
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 6 |
Uncertain significance | 0 | 14 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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20 |
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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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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 | IMAC |
SYNONYM | MIP-4a |
SYNONYM | MIP-4alpha |
SYNONYM | SCYA26 |
SYNONYM | TSC-1 |
MIM | 604697 OMIM |
HGNC | HGNC:10625 HGNC |
Ensembl | ENSG00000006606 Ensembl |
AllianceGenome | HGNC:10625 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000394905.2 | hg38 | chr7 | 75,769,533 | 75,789,896 | 20,364 |
ENST00000005180.9 | hg38 | chr7 | 75,769,538 | 75,772,211 | 2,674 |
ENST00000394905.2 | hg19 | chr7 | 75,398,851 | 75,419,214 | 20,364 |
ENST00000005180.9 | hg19 | chr7 | 75,398,856 | 75,401,529 | 2,674 |
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