PHOSPHO1 phosphoethanolamine/phosphocholine phosphatase 1
Information
- Symbol
- PHOSPHO1
- Type
- protein-coding
- Description
- phosphoethanolamine/phosphocholine phosphatase 1
- Entrez Gene ID
- 162466
- Genome
- hg19
- Position
- chr17:47,301,022-47,304,123
- Genome
- hg38
- Position
- chr17:49,223,660-49,226,761
- HGNC
- HGNC:16815 HGNC
- Ensembl
- ENSG00000173868 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 36 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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38 |
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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
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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 |
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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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000310544.9 | hg38 | chr17 | 49,223,366 | 49,230,787 | 7,422 |
ENST00000514112.1 | hg38 | chr17 | 49,223,660 | 49,226,761 | 3,102 |
ENST00000413580.5 | hg38 | chr17 | 49,223,370 | 49,230,766 | 7,397 |
ENST00000310544.9 | hg19 | chr17 | 47,300,728 | 47,308,149 | 7,422 |
ENST00000413580.5 | hg19 | chr17 | 47,300,732 | 47,308,128 | 7,397 |
ENST00000514112.1 | hg19 | chr17 | 47,301,022 | 47,304,123 | 3,102 |
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