RGD:11647122 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:11647122 -  Homo sapiens

RGD ID: 11647122
RS ID: rs886061791
ClinVar ID: CV308909
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LCA5  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 6 80,228,650
GRCh38 6 79,518,933
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_016011.1:g.23498T>C
NC_000006.12:g.79518933A>G
NC_000006.11:g.80228650A>G
NM_001122769.3:c.-39T>C
More... 		06/14/2016 5 prime utr variant uncertain significance Amaurosis congenita of Leber, type 5
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:LCA5
Accession:XM_011535504
Location:5UTRS;EXON

Gene Symbol:LCA5
Accession:NM_001122769
Location:5UTRS;EXON

Gene Symbol:LCA5
Accession:NM_181714
Location:5UTRS;EXON

Gene Symbol:LCA5
Accession:XM_047418251
Location:5UTRS;EXON

Gene Symbol:LCA5
Accession:XM_005248665
Location:5UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000274844 CLINVAR
dbSNP (RS) rs886061791 CLINVAR
MedGen C1858301 CLINVAR
NCBI Gene LCA5 CLINVAR
OMIM 604537 CLINVAR
  611408 CLINVAR