RAB30 RAB30, member RAS oncogene family
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 12 |
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
Search Word
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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Target data | : |
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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000534141.5 | hg38 | chr11 | 82,979,268 | 83,071,923 | 92,656 |
ENST00000525117.5 | hg38 | chr11 | 82,987,024 | 82,997,413 | 10,390 |
ENST00000527633.6 | hg38 | chr11 | 82,973,133 | 83,071,897 | 98,765 |
ENST00000532548.5 | hg38 | chr11 | 82,987,401 | 82,997,413 | 10,013 |
ENST00000260056.6 | hg38 | chr11 | 82,981,790 | 83,034,569 | 52,780 |
ENST00000612684.4 | hg38 | chr11 | 82,973,133 | 83,071,462 | 98,330 |
ENST00000533486.5 | hg38 | chr11 | 82,973,133 | 83,071,866 | 98,734 |
ENST00000612684.4 | hg19 | chr11 | 82,684,175 | 82,782,504 | 98,330 |
ENST00000533486.5 | hg19 | chr11 | 82,684,175 | 82,782,908 | 98,734 |
ENST00000527633.6 | hg19 | chr11 | 82,684,175 | 82,782,939 | 98,765 |
ENST00000534141.5 | hg19 | chr11 | 82,690,310 | 82,782,965 | 92,656 |
ENST00000260056.6 | hg19 | chr11 | 82,692,832 | 82,745,611 | 52,780 |
ENST00000525117.5 | hg19 | chr11 | 82,698,066 | 82,708,455 | 10,390 |
ENST00000532548.5 | hg19 | chr11 | 82,698,443 | 82,708,455 | 10,013 |
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