RRAS RAS related

Information
Symbol
RRAS
Type
protein-coding
Description
RAS related
Entrez Gene ID
6237
Genome
hg19
Position
chr19:50,138,549-50,143,400
Genome
hg38
Position
chr19:49,635,292-49,640,143
MIM
165090 OMIM
HGNC
HGNC:10447 HGNC
Ensembl
ENSG00000126458 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 54
Likely benign 0 220
Conflicting classifications of pathogenicity 0 24
Uncertain significance 0 290
Ranking
ClinVar
0
0
154
380
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 R-Ras
SYNONYM RRAS1
MIM 165090 OMIM
HGNC HGNC:10447 HGNC
Ensembl ENSG00000126458 Ensembl
AllianceGenome HGNC:10447
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000246792.4 hg38 chr19 49,635,292 49,640,143 4,852
ENST00000246792.4 hg19 chr19 50,138,549 50,143,400 4,852
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