RASD2 RASD family member 2

Information
Symbol
RASD2
Type
protein-coding
Description
RASD family member 2
Entrez Gene ID
23551
Genome
hg19
Position
chr22:35,936,878-35,950,046
Genome
hg38
Position
chr22:35,540,831-35,553,999
MIM
612842 OMIM
HGNC
HGNC:18229 HGNC
Ensembl
ENSG00000100302 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 20
Ranking
ClinVar
0
0
0
20
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 Rhes
SYNONYM TEM2
MIM 612842 OMIM
HGNC HGNC:18229 HGNC
Ensembl ENSG00000100302 Ensembl
AllianceGenome HGNC:18229
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000216127.5 hg38 chr22 35,540,831 35,553,999 13,169
ENST00000216127.5 hg19 chr22 35,936,878 35,950,046 13,169
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