CSF3 colony stimulating factor 3
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 12 |
Uncertain significance | 0 | 16 |
Ranking
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0 |
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28 |
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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
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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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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 | C17orf33 |
SYNONYM | CSF3OS |
SYNONYM | GCSF |
MIM | 138970 OMIM |
HGNC | HGNC:2438 HGNC |
Ensembl | ENSG00000108342 Ensembl |
AllianceGenome | HGNC:2438 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000331769.6 | hg38 | chr17 | 40,015,447 | 40,017,813 | 2,367 |
ENST00000225474.6 | hg38 | chr17 | 40,015,444 | 40,017,813 | 2,370 |
ENST00000577675.1 | hg38 | chr17 | 40,015,487 | 40,017,648 | 2,162 |
ENST00000394148.7 | hg38 | chr17 | 40,015,467 | 40,017,057 | 1,591 |
ENST00000394149.8 | hg38 | chr17 | 40,015,440 | 40,017,813 | 2,374 |
ENST00000394149.8 | hg19 | chr17 | 38,171,693 | 38,174,066 | 2,374 |
ENST00000225474.6 | hg19 | chr17 | 38,171,697 | 38,174,066 | 2,370 |
ENST00000331769.6 | hg19 | chr17 | 38,171,700 | 38,174,066 | 2,367 |
ENST00000394148.7 | hg19 | chr17 | 38,171,720 | 38,173,310 | 1,591 |
ENST00000577675.1 | hg19 | chr17 | 38,171,740 | 38,173,901 | 2,162 |
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