RHOQ ras homolog family member Q

Information
Symbol
RHOQ
Type
protein-coding
Description
ras homolog family member Q
Entrez Gene ID
23433
Genome
hg19
Position
chr2:46,769,629-46,811,827
Genome
hg38
Position
chr2:46,542,490-46,584,688
MIM
605857 OMIM
HGNC
HGNC:17736 HGNC
Ensembl
ENSG00000119729 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 26
Ranking
ClinVar
0
0
0
26
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 ARHQ
SYNONYM HEL-S-42
SYNONYM RASL7A
SYNONYM TC10
SYNONYM TC10A
MIM 605857 OMIM
HGNC HGNC:17736 HGNC
Ensembl ENSG00000119729 Ensembl
AllianceGenome HGNC:17736
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000238738.9 hg38 chr2 46,542,490 46,584,688 42,199
ENST00000238738.9 hg19 chr2 46,769,629 46,811,827 42,199
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