RAB39B RAB39B, member RAS oncogene family

Information
Symbol
RAB39B
Type
protein-coding
Description
RAB39B, member RAS oncogene family
Entrez Gene ID
116442
Genome
hg19
Position
chrX:154,487,520-154,493,776
Genome
hg38
Position
chrX:155,258,235-155,264,491
MIM
300774 OMIM
HGNC
HGNC:16499 HGNC
Ensembl
ENSG00000155961 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 14
Likely pathogenic 0 6
Benign 0 26
Likely benign 0 26
Conflicting classifications of pathogenicity 0 6
not provided 7 0
Uncertain significance 0 78
Ranking
ClinVar
0
0
12
126
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
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 BGMR
SYNONYM MRX72
SYNONYM WSMN
SYNONYM WSN
SYNONYM XLID72
MIM 300774 OMIM
HGNC HGNC:16499 HGNC
Ensembl ENSG00000155961 Ensembl
AllianceGenome HGNC:16499
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000369454.4 hg38 chrX 155,258,235 155,264,491 6,257
ENST00000369454.4 hg19 chrX 154,487,520 154,493,776 6,257
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