RAB17 RAB17, member RAS oncogene family

Information
Symbol
RAB17
Type
protein-coding
Description
RAB17, member RAS oncogene family
Entrez Gene ID
64284
Genome
hg19
Position
chr2:238,482,969-238,499,377
Genome
hg38
Position
chr2:237,574,326-237,590,734
MIM
602206 OMIM
HGNC
HGNC:16523 HGNC
Ensembl
ENSG00000124839 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 32
Ranking
ClinVar
0
0
0
34
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 602206 OMIM
HGNC HGNC:16523 HGNC
Ensembl ENSG00000124839 Ensembl
AllianceGenome HGNC:16523
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000409822.1 hg38 chr2 237,574,738 237,590,780 16,043
ENST00000409576.1 hg38 chr2 237,574,327 237,590,660 16,334
ENST00000264601.8 hg38 chr2 237,574,326 237,590,734 16,409
ENST00000264601.8 hg19 chr2 238,482,969 238,499,377 16,409
ENST00000409576.1 hg19 chr2 238,482,970 238,499,303 16,334
ENST00000409822.1 hg19 chr2 238,483,381 238,499,423 16,043
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