RHOG ras homolog family member G

Information
Symbol
RHOG
Type
protein-coding
Description
ras homolog family member G
Entrez Gene ID
391
Genome
hg19
Position
chr11:3,848,208-3,862,189
Genome
hg38
Position
chr11:3,826,978-3,840,959
MIM
179505 OMIM
HGNC
HGNC:672 HGNC
Ensembl
ENSG00000177105 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 8
Ranking
ClinVar
0
0
0
8
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
Category :
Search word :
Filtering :
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
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
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
TypeID
SYNONYM ARHG
MIM 179505 OMIM
HGNC HGNC:672 HGNC
Ensembl ENSG00000177105 Ensembl
AllianceGenome HGNC:672
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000351018.5 hg38 chr11 3,826,978 3,840,959 13,982
ENST00000533217.1 hg38 chr11 3,827,445 3,830,651 3,207
ENST00000396979.1 hg38 chr11 3,826,982 3,837,867 10,886
ENST00000396978.1 hg38 chr11 3,827,416 3,840,842 13,427
ENST00000351018.5 hg19 chr11 3,848,208 3,862,189 13,982
ENST00000396979.1 hg19 chr11 3,848,212 3,859,097 10,886
ENST00000396978.1 hg19 chr11 3,848,646 3,862,072 13,427
ENST00000533217.1 hg19 chr11 3,848,675 3,851,881 3,207
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