RGD:14693667 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:14693667 -  Homo sapiens

RGD ID: 14693667
RS ID: rs750388794
ClinVar ID: CV620750
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SUCLG1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 2 84,658,631
GRCh38 2 84,431,507
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_003849.4:c.825+1G>A
NG_016755.1:g.32956G>A
NC_000002.12:g.84431507C>T
NC_000002.11:g.84658631C>T
More... 		02/02/2019 splice donor variant conflicting interpretations of pathogenicity|uncertain significance Mitochondrial DNA depletion syndrome 9 (encephalomyopathic with methylmalonic aciduria)
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:SUCLG1
Accession:NM_003849
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:16199547   PMID:20693550   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000779336 CLINVAR
dbSNP (RS) rs750388794 CLINVAR
MedGen C3151476 CLINVAR
NCBI Gene SUCLG1 CLINVAR
OMIM 245400 CLINVAR
  611224 CLINVAR