RASL11B RAS like family 11 member B

Information
Symbol
RASL11B
Type
protein-coding
Description
RAS like family 11 member B
Entrez Gene ID
65997
Genome
hg19
Position
chr4:53,728,484-53,733,002
Genome
hg38
Position
chr4:52,862,317-52,866,835
MIM
612404 OMIM
HGNC
HGNC:23804 HGNC
Ensembl
ENSG00000128045 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 26
Ranking
ClinVar
0
0
0
26
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 :
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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
MIM 612404 OMIM
HGNC HGNC:23804 HGNC
Ensembl ENSG00000128045 Ensembl
AllianceGenome HGNC:23804
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000248706.5 hg38 chr4 52,862,317 52,866,835 4,519
ENST00000248706.5 hg19 chr4 53,728,484 53,733,002 4,519
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