EPOR erythropoietin receptor
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely pathogenic | 0 | 6 |
Benign | 4 | 62 |
Likely benign | 0 | 42 |
Affects | 0 | 10 |
Uncertain significance | 0 | 98 |
Ranking
ClinVar | |
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0 |
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0 |
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32 |
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164 |
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10 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
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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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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 | EPO-R |
MIM | 133171 OMIM |
HGNC | HGNC:3416 HGNC |
Ensembl | ENSG00000187266 Ensembl |
AllianceGenome | HGNC:3416 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000592375.6 | hg38 | chr19 | 11,377,625 | 11,384,312 | 6,688 |
ENST00000222139.11 | hg38 | chr19 | 11,377,207 | 11,384,314 | 7,108 |
ENST00000222139.11 | hg19 | chr19 | 11,487,883 | 11,494,990 | 7,108 |
ENST00000592375.6 | hg19 | chr19 | 11,488,301 | 11,494,988 | 6,688 |
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