RRAGD Ras related GTP binding D

Information
Symbol
RRAGD
Type
protein-coding
Description
Ras related GTP binding D
Entrez Gene ID
58528
Genome
hg19
Position
chr6:90,074,335-90,121,992
Genome
hg38
Position
chr6:89,364,616-89,412,273
MIM
608268 OMIM
HGNC
HGNC:19903 HGNC
Ensembl
ENSG00000025039 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 10
Likely pathogenic 0 2
Uncertain significance 0 20
Ranking
ClinVar
0
0
0
24
8
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 :
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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 HOMG7
SYNONYM RAGD
SYNONYM bA11D8.2.1
MIM 608268 OMIM
HGNC HGNC:19903 HGNC
Ensembl ENSG00000025039 Ensembl
AllianceGenome HGNC:19903
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000369415.9 hg38 chr6 89,364,616 89,412,273 47,658
ENST00000359203.3 hg38 chr6 89,364,998 89,412,070 47,073
ENST00000369415.9 hg19 chr6 90,074,335 90,121,992 47,658
ENST00000359203.3 hg19 chr6 90,074,717 90,121,789 47,073
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