RRAGB Ras related GTP binding B

Information
Symbol
RRAGB
Type
protein-coding
Description
Ras related GTP binding B
Entrez Gene ID
10325
Genome
hg19
Position
chrX:55,744,318-55,784,781
Genome
hg38
Position
chrX:55,717,885-55,758,348
MIM
300725 OMIM
HGNC
HGNC:19901 HGNC
Ensembl
ENSG00000083750 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 2
not provided 6 0
Uncertain significance 0 22
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
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 RAGB
SYNONYM bA465E19.1
MIM 300725 OMIM
HGNC HGNC:19901 HGNC
Ensembl ENSG00000083750 Ensembl
AllianceGenome HGNC:19901
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000262850.7 hg38 chrX 55,717,885 55,758,348 40,464
ENST00000374941.9 hg38 chrX 55,717,749 55,758,774 41,026
ENST00000374941.9 hg19 chrX 55,744,182 55,785,207 41,026
ENST00000262850.7 hg19 chrX 55,744,318 55,784,781 40,464
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