CPSF7 cleavage and polyadenylation specific factor 7
Information
- Symbol
- CPSF7
- Type
- protein-coding
- Description
- cleavage and polyadenylation specific factor 7
- Entrez Gene ID
- 79869
- Genome
- hg19
- Position
- chr11:61,170,113-61,197,383
- Genome
- hg38
- Position
- chr11:61,402,641-61,429,911
- HGNC
- HGNC:30098 HGNC
- Ensembl
- ENSG00000149532 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
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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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 |
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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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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 |
Type | ID |
---|---|
SYNONYM | CFIm59 |
HGNC | HGNC:30098 HGNC |
Ensembl | ENSG00000149532 Ensembl |
AllianceGenome | HGNC:30098 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000626926.1 | hg38 | chr11 | 61,421,225 | 61,429,235 | 8,011 |
ENST00000439958.8 | hg38 | chr11 | 61,402,729 | 61,429,975 | 27,247 |
ENST00000448745.5 | hg38 | chr11 | 61,404,419 | 61,429,304 | 24,886 |
ENST00000541963.5 | hg38 | chr11 | 61,419,970 | 61,429,948 | 9,979 |
ENST00000340437.8 | hg38 | chr11 | 61,402,641 | 61,429,911 | 27,271 |
ENST00000394888.8 | hg38 | chr11 | 61,402,649 | 61,430,031 | 27,383 |
ENST00000340437.8 | hg19 | chr11 | 61,170,113 | 61,197,383 | 27,271 |
ENST00000394888.8 | hg19 | chr11 | 61,170,121 | 61,197,503 | 27,383 |
ENST00000439958.8 | hg19 | chr11 | 61,170,201 | 61,197,447 | 27,247 |
ENST00000448745.5 | hg19 | chr11 | 61,171,891 | 61,196,776 | 24,886 |
ENST00000541963.5 | hg19 | chr11 | 61,187,442 | 61,197,420 | 9,979 |
ENST00000626926.1 | hg19 | chr11 | 61,188,697 | 61,196,707 | 8,011 |
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