RAB1B RAB1B, member RAS oncogene family
Information
Clinical Significance
MGeND | ClinVar | |
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Uncertain significance | 0 | 20 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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20 |
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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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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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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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MIM | 612565 OMIM |
HGNC | HGNC:18370 HGNC |
Ensembl | ENSG00000174903 Ensembl |
AllianceGenome | HGNC:18370 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000311481.11 | hg38 | chr11 | 66,268,639 | 66,277,492 | 8,854 |
ENST00000527397.1 | hg38 | chr11 | 66,268,590 | 66,276,629 | 8,040 |
ENST00000527397.1 | hg19 | chr11 | 66,036,061 | 66,044,100 | 8,040 |
ENST00000311481.11 | hg19 | chr11 | 66,036,110 | 66,044,963 | 8,854 |
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