GPR182 G protein-coupled receptor 182
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 26 |
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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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 | 7TMR |
SYNONYM | ADMR |
SYNONYM | AM-R |
SYNONYM | AMR |
SYNONYM | G10D |
SYNONYM | L1-R |
SYNONYM | gamrh |
SYNONYM | hrhAMR |
MIM | 605307 OMIM |
HGNC | HGNC:13708 HGNC |
Ensembl | ENSG00000166856 Ensembl |
AllianceGenome | HGNC:13708 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000622922.1 | hg38 | chr12 | 56,996,961 | 56,997,551 | 591 |
ENST00000300098.3 | hg38 | chr12 | 56,994,492 | 56,998,447 | 3,956 |
ENST00000300098.3 | hg19 | chr12 | 57,388,276 | 57,392,231 | 3,956 |
ENST00000622922.1 | hg19 | chr12 | 57,390,745 | 57,391,335 | 591 |
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