GCGR glucagon receptor
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 8 |
Benign | 0 | 54 |
Likely benign | 0 | 102 |
Conflicting classifications of pathogenicity | 0 | 4 |
Uncertain significance | 0 | 130 |
Ranking
ClinVar | |
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0 |
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0 |
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22 |
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262 |
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4 |
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 | GGR |
SYNONYM | GL-R |
SYNONYM | MVAH |
MIM | 138033 OMIM |
HGNC | HGNC:4192 HGNC |
Ensembl | ENSG00000215644 Ensembl |
AllianceGenome | HGNC:4192 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000570996.5 | hg38 | chr17 | 81,804,149 | 81,813,689 | 9,541 |
ENST00000400723.8 | hg38 | chr17 | 81,804,150 | 81,814,008 | 9,859 |
ENST00000570996.5 | hg19 | chr17 | 79,762,025 | 79,771,565 | 9,541 |
ENST00000400723.8 | hg19 | chr17 | 79,762,026 | 79,771,884 | 9,859 |
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