RAB5B RAB5B, member RAS oncogene family

Information
Symbol
RAB5B
Type
protein-coding
Description
RAB5B, member RAS oncogene family
Entrez Gene ID
5869
Genome
hg19
Position
chr12:56,367,862-56,390,467
Genome
hg38
Position
chr12:55,974,078-55,996,683
MIM
179514 OMIM
HGNC
HGNC:9784 HGNC
Ensembl
ENSG00000111540 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 14
Ranking
ClinVar
0
0
0
16
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
MIM 179514 OMIM
HGNC HGNC:9784 HGNC
Ensembl ENSG00000111540 Ensembl
AllianceGenome HGNC:9784
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000360299.10 hg38 chr12 55,974,078 55,996,683 22,606
ENST00000553116.5 hg38 chr12 55,973,913 55,994,706 20,794
ENST00000448789.2 hg38 chr12 55,974,101 55,993,086 18,986
ENST00000628569.1 hg38 chr12 55,986,961 55,992,212 5,252
ENST00000553116.5 hg19 chr12 56,367,697 56,388,490 20,794
ENST00000360299.10 hg19 chr12 56,367,862 56,390,467 22,606
ENST00000448789.2 hg19 chr12 56,367,885 56,386,870 18,986
ENST00000628569.1 hg19 chr12 56,380,745 56,385,996 5,252
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