RAB11B RAB11B, member RAS oncogene family

Information
Symbol
RAB11B
Type
protein-coding
Description
RAB11B, member RAS oncogene family
Entrez Gene ID
9230
Genome
hg19
Position
chr19:8,455,244-8,469,318
Genome
hg38
Position
chr19:8,390,360-8,404,434
MIM
604198 OMIM
HGNC
HGNC:9761 HGNC
Ensembl
ENSG00000185236 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 4
Likely pathogenic 0 6
Benign 0 76
Likely benign 0 224
Conflicting classifications of pathogenicity 0 4
Uncertain significance 0 118
Ranking
ClinVar
0
0
38
364
2
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 H-YPT3
SYNONYM NDAGSCW
MIM 604198 OMIM
HGNC HGNC:9761 HGNC
Ensembl ENSG00000185236 Ensembl
AllianceGenome HGNC:9761
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000601897.1 hg38 chr19 8,390,389 8,402,799 12,411
ENST00000594216.1 hg38 chr19 8,390,393 8,402,924 12,532
ENST00000328024.11 hg38 chr19 8,390,360 8,404,434 14,075
ENST00000328024.11 hg19 chr19 8,455,244 8,469,318 14,075
ENST00000601897.1 hg19 chr19 8,455,273 8,467,683 12,411
ENST00000594216.1 hg19 chr19 8,455,277 8,467,808 12,532
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