PLIN5 perilipin 5
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 10 |
Uncertain significance | 0 | 94 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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104 |
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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 | LSDA5 |
SYNONYM | LSDP5 |
SYNONYM | MLDP |
SYNONYM | OXPAT |
MIM | 613248 OMIM |
HGNC | HGNC:33196 HGNC |
Ensembl | ENSG00000214456 Ensembl |
AllianceGenome | HGNC:33196 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000586133.1 | hg38 | chr19 | 4,533,249 | 4,535,224 | 1,976 |
ENST00000592610.1 | hg38 | chr19 | 4,532,372 | 4,534,274 | 1,903 |
ENST00000381848.7 | hg38 | chr19 | 4,522,531 | 4,535,224 | 12,694 |
ENST00000381848.7 | hg19 | chr19 | 4,522,543 | 4,535,236 | 12,694 |
ENST00000592610.1 | hg19 | chr19 | 4,532,384 | 4,534,286 | 1,903 |
ENST00000586133.1 | hg19 | chr19 | 4,533,261 | 4,535,236 | 1,976 |
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