CSTF3 cleavage stimulation factor subunit 3
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 1 | 0 |
Uncertain significance | 0 | 30 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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30 |
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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
Locus Zoom
Variants
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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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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 | CSTF-77 |
MIM | 600367 OMIM |
HGNC | HGNC:2485 HGNC |
Ensembl | ENSG00000176102 Ensembl |
AllianceGenome | HGNC:2485 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000431742.2 | hg38 | chr11 | 33,141,465 | 33,161,491 | 20,027 |
ENST00000438862.6 | hg38 | chr11 | 33,140,966 | 33,161,531 | 20,566 |
ENST00000323959.9 | hg38 | chr11 | 33,084,584 | 33,161,480 | 76,897 |
ENST00000524827.6 | hg38 | chr11 | 33,084,595 | 33,161,494 | 76,900 |
ENST00000323959.9 | hg19 | chr11 | 33,106,130 | 33,183,026 | 76,897 |
ENST00000524827.6 | hg19 | chr11 | 33,106,141 | 33,183,040 | 76,900 |
ENST00000438862.6 | hg19 | chr11 | 33,162,512 | 33,183,077 | 20,566 |
ENST00000431742.2 | hg19 | chr11 | 33,163,011 | 33,183,037 | 20,027 |
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