RHOV ras homolog family member V

Information
Symbol
RHOV
Type
protein-coding
Description
ras homolog family member V
Entrez Gene ID
171177
Genome
hg19
Position
chr15:41,164,412-41,166,432
Genome
hg38
Position
chr15:40,872,214-40,874,234
MIM
620101 OMIM
HGNC
HGNC:18313 HGNC
Ensembl
ENSG00000104140 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 10
Ranking
ClinVar
0
0
0
12
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 :
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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
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 ARHV
SYNONYM CHP
SYNONYM WRCH2
MIM 620101 OMIM
HGNC HGNC:18313 HGNC
Ensembl ENSG00000104140 Ensembl
AllianceGenome HGNC:18313
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000220507.5 hg38 chr15 40,872,214 40,874,234 2,021
ENST00000220507.5 hg19 chr15 41,164,412 41,166,432 2,021
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