RAB5C RAB5C, member RAS oncogene family

Information
Symbol
RAB5C
Type
protein-coding
Description
RAB5C, member RAS oncogene family
Entrez Gene ID
5878
Genome
hg19
Position
chr17:40,277,685-40,307,006
Genome
hg38
Position
chr17:42,125,667-42,154,988
MIM
604037 OMIM
HGNC
HGNC:9785 HGNC
Ensembl
ENSG00000108774 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Uncertain significance 0 22
Ranking
ClinVar
0
0
2
22
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
SYNONYM L1880
SYNONYM RAB5CL
SYNONYM RAB5L
SYNONYM RABL
MIM 604037 OMIM
HGNC HGNC:9785 HGNC
Ensembl ENSG00000108774 Ensembl
AllianceGenome HGNC:9785
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000393860.7 hg38 chr17 42,124,978 42,155,044 30,067
ENST00000346213.9 hg38 chr17 42,124,979 42,154,989 30,011
ENST00000547517.5 hg38 chr17 42,125,667 42,154,988 29,322
ENST00000393860.7 hg19 chr17 40,276,996 40,307,062 30,067
ENST00000346213.9 hg19 chr17 40,276,997 40,307,007 30,011
ENST00000547517.5 hg19 chr17 40,277,685 40,307,006 29,322
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