RASL10B RAS like family 10 member B

Information
Symbol
RASL10B
Type
protein-coding
Description
RAS like family 10 member B
Entrez Gene ID
91608
Genome
hg19
Position
chr17:34,058,658-34,070,540
Genome
hg38
Position
chr17:35,731,639-35,743,521
MIM
612128 OMIM
HGNC
HGNC:30295 HGNC
Ensembl
ENSG00000270885 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 14
Ranking
ClinVar
0
0
0
14
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 :
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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 RRP17
SYNONYM VTS58635
MIM 612128 OMIM
HGNC HGNC:30295 HGNC
Ensembl ENSG00000270885 Ensembl
AllianceGenome HGNC:30295
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000603017.2 hg38 chr17 35,731,639 35,743,521 11,883
ENST00000603017.2 hg19 chr17 34,058,658 34,070,540 11,883
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