RAP2B RAP2B, member of RAS oncogene family

Information
Symbol
RAP2B
Type
protein-coding
Description
RAP2B, member of RAS oncogene family
Entrez Gene ID
5912
Genome
hg19
Position
chr3:152,880,015-152,888,416
Genome
hg38
Position
chr3:153,162,226-153,170,627
MIM
179541 OMIM
HGNC
HGNC:9862 HGNC
Ensembl
ENSG00000181467 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 6
Ranking
ClinVar
0
0
0
8
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 :
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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
MIM 179541 OMIM
HGNC HGNC:9862 HGNC
Ensembl ENSG00000181467 Ensembl
AllianceGenome HGNC:9862
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000323534.5 hg38 chr3 153,162,226 153,170,627 8,402
ENST00000323534.5 hg19 chr3 152,880,015 152,888,416 8,402
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