PLCB2 phospholipase C beta 2
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 8 |
Likely benign | 0 | 12 |
Uncertain significance | 0 | 110 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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126 |
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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 |
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 | PLC-beta-2 |
MIM | 604114 OMIM |
HGNC | HGNC:9055 HGNC |
Ensembl | ENSG00000137841 Ensembl |
AllianceGenome | HGNC:9055 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000557821.5 | hg38 | chr15 | 40,287,909 | 40,307,837 | 19,929 |
ENST00000260402.8 | hg38 | chr15 | 40,287,909 | 40,307,935 | 20,027 |
ENST00000456256.6 | hg38 | chr15 | 40,288,139 | 40,307,825 | 19,687 |
ENST00000543785.3 | hg38 | chr15 | 40,300,667 | 40,307,910 | 7,244 |
ENST00000557821.5 | hg19 | chr15 | 40,580,110 | 40,600,038 | 19,929 |
ENST00000260402.8 | hg19 | chr15 | 40,580,110 | 40,600,136 | 20,027 |
ENST00000456256.6 | hg19 | chr15 | 40,580,340 | 40,600,026 | 19,687 |
ENST00000543785.3 | hg19 | chr15 | 40,592,868 | 40,600,111 | 7,244 |
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