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 Behavioral & Substance Use Disorder 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 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
Advanced Search (OLGA)
Variants search result for All species
(View Results for all Objects and Ontologies)

7 records found for search term Tomm6
Refine Term:
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
329349459CV2431793single nucleotide variantNM_001382294.1(TOMM6):c.26G>A (p.Ser9Asn)not specified [RCV004248952]likely benign64178772341787723Humanname
401746311CV2713001single nucleotide variantNM_001382294.1(TOMM6):c.22G>T (p.Val8Leu)not specified [RCV004314706]uncertain significance64178771941787719Humanname
597689055CV3614332single nucleotide variantNM_001382294.1(TOMM6):c.22G>C (p.Val8Leu)not specified [RCV004875402]uncertain significance64178771941787719Humanname
401748006CV2716393single nucleotide variantNM_001382294.1(TOMM6):c.97C>A (p.Arg33Ser)not specified [RCV004325382]uncertain significance64178779441787794Humanname
401858134CV2757662single nucleotide variantNM_001382294.1(TOMM6):c.60A>G (p.Ile20Met)not specified [RCV004334774]uncertain significance64178775741787757Humanname
156188778CV2328692single nucleotide variantNM_001382294.1(TOMM6):c.199C>G (p.Leu67Val)not specified [RCV004177931]uncertain significance64178930241789302Humanname
401748509CV2726931single nucleotide variantNM_001382294.1(TOMM6):c.218G>A (p.Gly73Glu)not specified [RCV004323214]uncertain significance64178932141789321Humanname