RHOD ras homolog family member D

Information
Symbol
RHOD
Type
protein-coding
Description
ras homolog family member D
Entrez Gene ID
29984
Genome
hg19
Position
chr11:66,824,318-66,839,488
Genome
hg38
Position
chr11:67,056,847-67,072,017
MIM
605781 OMIM
HGNC
HGNC:670 HGNC
Ensembl
ENSG00000173156 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Uncertain significance 0 16
Ranking
ClinVar
0
0
0
18
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 ARHD
SYNONYM RHOHP1
SYNONYM RHOM
SYNONYM Rho
MIM 605781 OMIM
HGNC HGNC:670 HGNC
Ensembl ENSG00000173156 Ensembl
AllianceGenome HGNC:670
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000308831.7 hg38 chr11 67,056,847 67,072,017 15,171
ENST00000532559.1 hg38 chr11 67,056,889 67,071,691 14,803
ENST00000308831.7 hg19 chr11 66,824,318 66,839,488 15,171
ENST00000532559.1 hg19 chr11 66,824,360 66,839,162 14,803
Genome browser