P2RY10 P2Y receptor family member 10
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 2 |
not provided | 6 | 0 |
Uncertain significance | 0 | 14 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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18 |
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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
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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Category | : |
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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 | LPS2 |
SYNONYM | LYPSR2 |
SYNONYM | P2Y10 |
MIM | 300529 OMIM |
HGNC | HGNC:19906 HGNC |
Ensembl | ENSG00000078589 Ensembl |
AllianceGenome | HGNC:19906 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000544091.1 | hg38 | chrX | 78,945,332 | 78,961,940 | 16,609 |
ENST00000171757.3 | hg38 | chrX | 78,945,391 | 78,963,727 | 18,337 |
ENST00000544091.1 | hg19 | chrX | 78,200,829 | 78,217,437 | 16,609 |
ENST00000171757.3 | hg19 | chrX | 78,200,888 | 78,219,224 | 18,337 |
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