PLIN2 perilipin 2
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 44 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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50 |
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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
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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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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 | ADFP |
SYNONYM | ADRP |
MIM | 103195 OMIM |
HGNC | HGNC:248 HGNC |
Ensembl | ENSG00000147872 Ensembl |
AllianceGenome | HGNC:248 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000380464.7 | hg38 | chr9 | 19,123,313 | 19,127,490 | 4,178 |
ENST00000380465.7 | hg38 | chr9 | 19,123,235 | 19,127,476 | 4,242 |
ENST00000276914.7 | hg38 | chr9 | 19,115,761 | 19,127,492 | 11,732 |
ENST00000276914.7 | hg19 | chr9 | 19,115,759 | 19,127,490 | 11,732 |
ENST00000380465.7 | hg19 | chr9 | 19,123,233 | 19,127,474 | 4,242 |
ENST00000380464.7 | hg19 | chr9 | 19,123,311 | 19,127,488 | 4,178 |
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