PLA2G4C phospholipase A2 group IVC
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 8 |
Likely benign | 0 | 4 |
Uncertain significance | 0 | 90 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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102 |
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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
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 |
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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 | CPLA2-gamma |
MIM | 603602 OMIM |
HGNC | HGNC:9037 HGNC |
Ensembl | ENSG00000105499 Ensembl |
AllianceGenome | HGNC:9037 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000599111.5 | hg38 | chr19 | 48,047,843 | 48,110,817 | 62,975 |
ENST00000599921.6 | hg38 | chr19 | 48,047,846 | 48,110,817 | 62,972 |
ENST00000354276.7 | hg38 | chr19 | 48,047,844 | 48,110,782 | 62,939 |
ENST00000354276.7 | hg19 | chr19 | 48,551,101 | 48,614,039 | 62,939 |
ENST00000599111.5 | hg19 | chr19 | 48,551,100 | 48,614,074 | 62,975 |
ENST00000599921.6 | hg19 | chr19 | 48,551,103 | 48,614,074 | 62,972 |
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