PTGIR prostaglandin I2 receptor
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 6 |
Uncertain significance | 0 | 54 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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64 |
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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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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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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 | PRIPR |
SYNONYM | IP |
MIM | 600022 OMIM |
HGNC | HGNC:9602 HGNC |
Ensembl | ENSG00000160013 Ensembl |
AllianceGenome | HGNC:9602 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000598865.5 | hg38 | chr19 | 46,621,167 | 46,625,072 | 3,906 |
ENST00000597185.1 | hg38 | chr19 | 46,621,167 | 46,625,072 | 3,906 |
ENST00000594275.1 | hg38 | chr19 | 46,621,167 | 46,625,072 | 3,906 |
ENST00000596260.1 | hg38 | chr19 | 46,623,130 | 46,625,037 | 1,908 |
ENST00000291294.7 | hg38 | chr19 | 46,620,468 | 46,625,089 | 4,622 |
ENST00000291294.7 | hg19 | chr19 | 47,123,725 | 47,128,346 | 4,622 |
ENST00000594275.1 | hg19 | chr19 | 47,124,424 | 47,128,329 | 3,906 |
ENST00000597185.1 | hg19 | chr19 | 47,124,424 | 47,128,329 | 3,906 |
ENST00000598865.5 | hg19 | chr19 | 47,124,424 | 47,128,329 | 3,906 |
ENST00000596260.1 | hg19 | chr19 | 47,126,387 | 47,128,294 | 1,908 |
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