PLA2G1B phospholipase A2 group IB
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 2 |
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
[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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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 | PLA2 |
SYNONYM | PLA2A |
SYNONYM | PPLA2 |
MIM | 172410 OMIM |
HGNC | HGNC:9030 HGNC |
Ensembl | ENSG00000170890 Ensembl |
AllianceGenome | HGNC:9030 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000549767.1 | hg38 | chr12 | 120,322,117 | 120,326,093 | 3,977 |
ENST00000423423.3 | hg38 | chr12 | 120,322,115 | 120,327,779 | 5,665 |
ENST00000308366.9 | hg38 | chr12 | 120,322,115 | 120,327,779 | 5,665 |
ENST00000308366.9 | hg19 | chr12 | 120,759,918 | 120,765,582 | 5,665 |
ENST00000423423.3 | hg19 | chr12 | 120,759,918 | 120,765,582 | 5,665 |
ENST00000549767.1 | hg19 | chr12 | 120,759,920 | 120,763,896 | 3,977 |
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