RAB13 RAB13, member RAS oncogene family
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 10 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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12 |
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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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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 |
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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 | GIG4 |
MIM | 602672 OMIM |
HGNC | HGNC:9762 HGNC |
Ensembl | ENSG00000143545 Ensembl |
AllianceGenome | HGNC:9762 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000614713.4 | hg38 | chr1 | 153,981,617 | 153,985,366 | 3,750 |
ENST00000368575.5 | hg38 | chr1 | 153,981,650 | 153,986,339 | 4,690 |
ENST00000614713.4 | hg19 | chr1 | 153,954,093 | 153,957,842 | 3,750 |
ENST00000368575.5 | hg19 | chr1 | 153,954,126 | 153,958,815 | 4,690 |
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