RGD:13782635 Rat Genome Database

Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models   new Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources

Variant: RGD:13782635 -  Homo sapiens

RGD ID: 13782635
RS ID: rs1554448791
ClinVar ID: CV544744
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CLN8  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 8 1,719,097
GRCh38 8 1,770,931
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_018941.3:c.-123-1G>C
LRG_691t1:c.-123-1G>C
NC_000008.10:g.1719097G>C
LRG_691:g.20154G>C
More... 		11/14/2017 splice acceptor variant uncertain significance CLN8-Related Neuronal Ceroid-Lipofuscinosis
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:CLN8
Accession:XM_047421513
Location:5UTRS;INTRON

Gene Symbol:CLN8
Accession:XM_011534745
Location:5UTRS;INTRON

Gene Symbol:CLN8
Accession:XM_005266021
Location:5UTRS;INTRON

Gene Symbol:CLN8
Accession:XM_011534746
Location:5UTRS;INTRON

Gene Symbol:CLN8
Accession:XM_011534747
Location:5UTRS;INTRON

Gene Symbol:CLN8
Accession:XM_047421512
Location:5UTRS;INTRON

Gene Symbol:CLN8
Accession:XM_005266023
Location:5UTRS;INTRON

Gene Symbol:CLN8
Accession:XM_005266022
Location:5UTRS;INTRON

Gene Symbol:CLN8
Accession:NM_018941
Location:5UTRS;INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000669108 CLINVAR
dbSNP (RS) rs1554448791 CLINVAR
MedGen C1838570 CLINVAR
NCBI Gene CLN8 CLINVAR
OMIM 600143 CLINVAR
  607837 CLINVAR