CYTH4 cytohesin 4
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Likely benign | 0 | 4 |
Uncertain significance | 0 | 40 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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50 |
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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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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 | CYT4 |
SYNONYM | DJ63G5.1 |
SYNONYM | PSCD4 |
SYNONYM | cytohesin-4 |
MIM | 606514 OMIM |
HGNC | HGNC:9505 HGNC |
Ensembl | ENSG00000100055 Ensembl |
AllianceGenome | HGNC:9505 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000405206.3 | hg38 | chr22 | 37,282,487 | 37,300,271 | 17,785 |
ENST00000402997.5 | hg38 | chr22 | 37,282,475 | 37,300,173 | 17,699 |
ENST00000248901.11 | hg38 | chr22 | 37,282,508 | 37,315,341 | 32,834 |
ENST00000402997.5 | hg19 | chr22 | 37,678,516 | 37,696,214 | 17,699 |
ENST00000405206.3 | hg19 | chr22 | 37,678,528 | 37,696,312 | 17,785 |
ENST00000248901.11 | hg19 | chr22 | 37,678,549 | 37,711,382 | 32,834 |
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