GPR17 G protein-coupled receptor 17
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 42 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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48 |
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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 |
Search Word
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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000393018.3 | hg38 | chr2 | 127,649,939 | 127,651,755 | 1,817 |
ENST00000272644.7 | hg38 | chr2 | 127,646,172 | 127,652,639 | 6,468 |
ENST00000486700.2 | hg38 | chr2 | 127,646,153 | 127,652,639 | 6,487 |
ENST00000544369.5 | hg38 | chr2 | 127,645,864 | 127,652,638 | 6,775 |
ENST00000544369.5 | hg19 | chr2 | 128,403,439 | 128,410,212 | 6,774 |
ENST00000486700.2 | hg19 | chr2 | 128,403,728 | 128,410,213 | 6,486 |
ENST00000272644.7 | hg19 | chr2 | 128,403,747 | 128,410,213 | 6,467 |
ENST00000393018.3 | hg19 | chr2 | 128,407,514 | 128,409,329 | 1,816 |
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