RAB29 RAB29, member RAS oncogene family

Information
Symbol
RAB29
Type
protein-coding
Description
RAB29, member RAS oncogene family
Entrez Gene ID
8934
Genome
hg19
Position
chr1:205,737,114-205,744,610
Genome
hg38
Position
chr1:205,767,986-205,775,482
MIM
603949 OMIM
HGNC
HGNC:9789 HGNC
Ensembl
ENSG00000117280 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
not provided 1 0
Uncertain significance 0 20
Ranking
ClinVar
0
0
0
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
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 RAB7L
SYNONYM RAB7L1
MIM 603949 OMIM
HGNC HGNC:9789 HGNC
Ensembl ENSG00000117280 Ensembl
AllianceGenome HGNC:9789
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000437324.6 hg38 chr1 205,769,703 205,775,451 5,749
ENST00000446390.6 hg38 chr1 205,769,718 205,775,233 5,516
ENST00000235932.8 hg38 chr1 205,769,437 205,775,449 6,013
ENST00000414729.1 hg38 chr1 205,770,300 205,775,459 5,160
ENST00000367139.8 hg38 chr1 205,767,986 205,775,482 7,497
ENST00000367139.8 hg19 chr1 205,737,114 205,744,610 7,497
ENST00000235932.8 hg19 chr1 205,738,565 205,744,577 6,013
ENST00000437324.6 hg19 chr1 205,738,831 205,744,579 5,749
ENST00000446390.6 hg19 chr1 205,738,846 205,744,361 5,516
ENST00000414729.1 hg19 chr1 205,739,428 205,744,587 5,160
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