CPSF4L cleavage and polyadenylation specific factor 4 like
Information
- Symbol
- CPSF4L
- Type
- protein-coding
- Description
- cleavage and polyadenylation specific factor 4 like
- Entrez Gene ID
- 642843
- Genome
- hg19
- Position
- chr17:71,244,588-71,258,019
- Genome
- hg38
- Position
- chr17:73,248,449-73,261,880
- HGNC
- HGNC:33632 HGNC
- Ensembl
- ENSG00000187959 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 26 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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26 |
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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 |
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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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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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ENST00000344935.8 | hg38 | chr17 | 73,248,449 | 73,261,880 | 13,432 |
ENST00000397671.1 | hg38 | chr17 | 73,249,793 | 73,262,352 | 12,560 |
ENST00000344935.8 | hg19 | chr17 | 71,244,588 | 71,258,019 | 13,432 |
ENST00000397671.1 | hg19 | chr17 | 71,245,932 | 71,258,491 | 12,560 |
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