RINL Ras and Rab interactor like

Information
Symbol
RINL
Type
protein-coding
Description
Ras and Rab interactor like
Entrez Gene ID
126432
Genome
hg19
Position
chr19:39,358,470-39,368,915
Genome
hg38
Position
chr19:38,867,830-38,878,275
MIM
620678 OMIM
HGNC
HGNC:24795 HGNC
Ensembl
ENSG00000187994 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 12
Uncertain significance 0 64
Ranking
ClinVar
0
0
0
78
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 620678 OMIM
HGNC HGNC:24795 HGNC
Ensembl ENSG00000187994 Ensembl
AllianceGenome HGNC:24795
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000591812.2 hg38 chr19 38,867,830 38,878,275 10,446
ENST00000598904.5 hg38 chr19 38,868,982 38,876,781 7,800
ENST00000591812.2 hg19 chr19 39,358,470 39,368,915 10,446
ENST00000598904.5 hg19 chr19 39,359,622 39,367,421 7,800
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