CYTH2 cytohesin 2
Clinical Significance
MGeND | ClinVar | |
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Uncertain significance | 0 | 18 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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18 |
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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 | ARNO |
SYNONYM | CTS18 |
SYNONYM | CTS18.1 |
SYNONYM | PSCD2 |
SYNONYM | PSCD2L |
SYNONYM | SEC7L |
SYNONYM | Sec7p-L |
SYNONYM | Sec7p-like |
SYNONYM | cytohesin-2 |
MIM | 602488 OMIM |
HGNC | HGNC:9502 HGNC |
Ensembl | ENSG00000105443 Ensembl |
AllianceGenome | HGNC:9502 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000704950.1 | hg38 | chr19 | 48,469,369 | 48,482,314 | 12,946 |
ENST00000452733.7 | hg38 | chr19 | 48,469,369 | 48,482,314 | 12,946 |
ENST00000641098.1 | hg38 | chr19 | 48,469,433 | 48,480,653 | 11,221 |
ENST00000427476.4 | hg38 | chr19 | 48,469,208 | 48,482,313 | 13,106 |
ENST00000427476.4 | hg19 | chr19 | 48,972,465 | 48,985,570 | 13,106 |
ENST00000452733.7 | hg19 | chr19 | 48,972,626 | 48,985,571 | 12,946 |
ENST00000704950.1 | hg19 | chr19 | 48,972,626 | 48,985,571 | 12,946 |
ENST00000641098.1 | hg19 | chr19 | 48,972,690 | 48,983,910 | 11,221 |
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