RAB34 RAB34, member RAS oncogene family

Information
Symbol
RAB34
Type
protein-coding
Description
RAB34, member RAS oncogene family
Entrez Gene ID
83871
Genome
hg19
Position
chr17:27,041,299-27,045,286
Genome
hg38
Position
chr17:28,714,281-28,718,268
MIM
610917 OMIM
HGNC
HGNC:16519 HGNC
Ensembl
ENSG00000109113 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 4
Likely pathogenic 0 4
Likely benign 0 4
Uncertain significance 0 32
Ranking
ClinVar
0
0
0
40
4
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
SYNONYM NARR
SYNONYM OFD20
SYNONYM RAB39
SYNONYM RAH
MIM 610917 OMIM
HGNC HGNC:16519 HGNC
Ensembl ENSG00000109113 Ensembl
AllianceGenome HGNC:16519
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000636772.1 hg38 chr17 28,714,793 28,717,850 3,058
ENST00000453384.7 hg38 chr17 28,714,281 28,718,268 3,988
ENST00000301043.10 hg38 chr17 28,714,284 28,718,415 4,132
ENST00000436730.7 hg38 chr17 28,714,625 28,718,161 3,537
ENST00000415040.6 hg38 chr17 28,714,285 28,718,183 3,899
ENST00000395243.7 hg38 chr17 28,714,284 28,717,748 3,465
ENST00000395245.9 hg38 chr17 28,714,284 28,717,868 3,585
ENST00000636513.1 hg38 chr17 28,715,032 28,717,708 2,677
ENST00000636154.2 hg38 chr17 28,715,829 28,717,708 1,880
ENST00000625712.2 hg38 chr17 28,714,284 28,718,166 3,883
ENST00000450529.5 hg38 chr17 28,714,285 28,718,166 3,882
ENST00000395243.7 hg19 chr17 27,041,302 27,044,766 3,465
ENST00000395245.9 hg19 chr17 27,041,302 27,044,886 3,585
ENST00000301043.10 hg19 chr17 27,041,302 27,045,433 4,132
ENST00000436730.7 hg19 chr17 27,041,643 27,045,179 3,537
ENST00000415040.6 hg19 chr17 27,041,303 27,045,201 3,899
ENST00000450529.5 hg19 chr17 27,041,303 27,045,184 3,882
ENST00000453384.7 hg19 chr17 27,041,299 27,045,286 3,988
ENST00000625712.2 hg19 chr17 27,041,302 27,045,184 3,883
ENST00000636154.2 hg19 chr17 27,042,847 27,044,726 1,880
ENST00000636513.1 hg19 chr17 27,042,050 27,044,726 2,677
ENST00000636772.1 hg19 chr17 27,041,811 27,044,868 3,058
Genome browser