RHOB ras homolog family member B
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Conflicting classifications of pathogenicity | 0 | 2 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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0 |
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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 |
Prediction | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | ARH6 |
| SYNONYM | ARHB |
| SYNONYM | MST081 |
| SYNONYM | MSTP081 |
| SYNONYM | RHOH6 |
| MIM | 165370 OMIM |
| HGNC | HGNC:668 HGNC |
| Ensembl | ENSG00000143878 Ensembl |
| AllianceGenome | HGNC:668 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000272233.6 | hg38 | chr2 | 20,447,074 | 20,449,440 | 2,367 |
| ENST00000272233.6 | hg19 | chr2 | 20,646,835 | 20,649,201 | 2,367 |
| Key | Value |
|---|---|
| strand | + |
| UniProt | TSG |
| start | 20,646,831 |
| Gene Symbol | RHOB |
| Entrez GeneId | 388 |
| Chr Band | 2p24 |
| end | 20,649,203 |
| chr | chr2 |
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