PPM1N protein phosphatase, Mg2+/Mn2+ dependent 1N (putative)
Information
- Symbol
- PPM1N
- Type
- protein-coding
- Description
- protein phosphatase, Mg2+/Mn2+ dependent 1N (putative)
- Entrez Gene ID
- 147699
- Genome
- hg19
- Position
- chr19:46,001,701-46,005,771
- Genome
- hg38
- Position
- chr19:45,498,443-45,502,513
- HGNC
- HGNC:26845 HGNC
- Ensembl
- ENSG00000213889 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 8 |
Likely pathogenic | 0 | 18 |
Benign | 0 | 66 |
Likely benign | 0 | 128 |
Conflicting classifications of pathogenicity | 0 | 20 |
Uncertain significance | 0 | 244 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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56 |
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386 |
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2 |
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 |
Search Word
Target data | : |
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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
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 |
---|---|---|---|---|---|
ENST00000401593.5 | hg38 | chr19 | 45,499,949 | 45,502,310 | 2,362 |
ENST00000451287.7 | hg38 | chr19 | 45,498,443 | 45,502,513 | 4,071 |
ENST00000401705.5 | hg38 | chr19 | 45,488,777 | 45,502,299 | 13,523 |
ENST00000396736.2 | hg38 | chr19 | 45,499,961 | 45,502,310 | 2,350 |
ENST00000396735.6 | hg38 | chr19 | 45,499,610 | 45,502,510 | 2,901 |
ENST00000396737.6 | hg38 | chr19 | 45,497,251 | 45,502,510 | 5,260 |
ENST00000456399.6 | hg38 | chr19 | 45,497,231 | 45,502,302 | 5,072 |
ENST00000401705.5 | hg19 | chr19 | 45,992,035 | 46,005,557 | 13,523 |
ENST00000456399.6 | hg19 | chr19 | 46,000,489 | 46,005,560 | 5,072 |
ENST00000396737.6 | hg19 | chr19 | 46,000,509 | 46,005,768 | 5,260 |
ENST00000451287.7 | hg19 | chr19 | 46,001,701 | 46,005,771 | 4,071 |
ENST00000396735.6 | hg19 | chr19 | 46,002,868 | 46,005,768 | 2,901 |
ENST00000401593.5 | hg19 | chr19 | 46,003,207 | 46,005,568 | 2,362 |
ENST00000396736.2 | hg19 | chr19 | 46,003,219 | 46,005,568 | 2,350 |
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