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 Homo sapiens
(View Results for all Objects and Ontologies)

26 records found for search term Slc25a28
Refine Term:
Assembly:
    Chr  
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156143601CV2200099single nucleotide variantNM_031212.4(SLC25A28):c.32T>G (p.Val11Gly)not specified [RCV004069677]uncertain significance109962030499620304Humanname
156051342CV2328948single nucleotide variantNM_031212.4(SLC25A28):c.80C>T (p.Ala27Val)not specified [RCV004180248]uncertain significance109962025699620256Humanname
405768054CV3325505single nucleotide variantNM_031212.4(SLC25A28):c.35C>T (p.Ala12Val)not specified [RCV004456487]uncertain significance109962030199620301Humanname
405768059CV3325506single nucleotide variantNM_031212.4(SLC25A28):c.43C>T (p.Pro15Ser)not specified [RCV004456488]uncertain significance109962029399620293Humanname
597700424CV3606320single nucleotide variantNM_031212.4(SLC25A28):c.79G>A (p.Ala27Thr)not specified [RCV004859864]uncertain significance109962025799620257Humanname
597754712CV3606321single nucleotide variantNM_031212.4(SLC25A28):c.41G>A (p.Gly14Glu)not specified [RCV004867960]uncertain significance109962029599620295Humanname
156035561CV2338929single nucleotide variantNM_031212.4(SLC25A28):c.178G>A (p.Gly60Ser)not specified [RCV004184519]uncertain significance109962015899620158Humanname
156065110CV2348731single nucleotide variantNM_031212.4(SLC25A28):c.134A>G (p.Glu45Gly)not specified [RCV004201141]uncertain significance109962020299620202Humanname
156174249CV2352170single nucleotide variantNM_031212.4(SLC25A28):c.110T>G (p.Val37Gly)not specified [RCV004200659]uncertain significance109962022699620226Humanname
155989337CV2352199single nucleotide variantNM_031212.4(SLC25A28):c.134A>C (p.Glu45Ala)not specified [RCV004200684]uncertain significance109962020299620202Humanname
156070781CV2354227single nucleotide variantNM_031212.4(SLC25A28):c.134A>T (p.Glu45Val)not specified [RCV004206652]uncertain significance109962020299620202Humanname
405768028CV3325501single nucleotide variantNM_031212.4(SLC25A28):c.116G>T (p.Arg39Leu)not specified [RCV004456483]uncertain significance109962022099620220Humanname
405768034CV3325502single nucleotide variantNM_031212.4(SLC25A28):c.121G>A (p.Ala41Thr)not specified [RCV004456484]uncertain significance109962021599620215Humanname
405768042CV3325503single nucleotide variantNM_031212.4(SLC25A28):c.122C>G (p.Ala41Gly)not specified [RCV004456485]uncertain significance109962021499620214Humanname
405768048CV3325504single nucleotide variantNM_031212.4(SLC25A28):c.151C>G (p.Pro51Ala)not specified [RCV004456486]uncertain significance109962018599620185Humanname
156170908CV2267586single nucleotide variantNM_031212.4(SLC25A28):c.820G>A (p.Val274Ile)not specified [RCV004134149]uncertain significance109961112499611124Humanname
155905996CV2283278single nucleotide variantNM_031212.4(SLC25A28):c.952G>A (p.Val318Ile)not provided [RCV004695489]|not specified [RCV004145944]uncertain significance109961099299610992Humanname
405768066CV3325507single nucleotide variantNM_031212.4(SLC25A28):c.964A>G (p.Thr322Ala)not specified [RCV004456489]uncertain significance109961098099610980Humanname
407451243CV3473985single nucleotide variantNM_031212.4(SLC25A28):c.371C>T (p.Thr124Met)not specified [RCV004683602]uncertain significance109961384599613845Humanname
597754701CV3606317single nucleotide variantNM_031212.4(SLC25A28):c.908G>A (p.Gly303Glu)not specified [RCV004867957]uncertain significance109961103699611036Humanname
597754705CV3606318single nucleotide variantNM_031212.4(SLC25A28):c.911A>G (p.His304Arg)not specified [RCV004867958]uncertain significance109961103399611033Humanname
597754708CV3606319single nucleotide variantNM_031212.4(SLC25A28):c.421G>A (p.Ala141Thr)not specified [RCV004867959]uncertain significance109961379599613795Humanname
598168733CV3918201single nucleotide variantNM_031212.4(SLC25A28):c.706G>A (p.Val236Ile)not specified [RCV005284148]uncertain significance109961123899611238Humanname
8633458CV88673single nucleotide variantNM_031212.3(SLC25A28):c.328C>T (p.Arg110Cys)Malignant melanoma [RCV000068766]not provided109961388899613888Humanname
401727121CV2684478single nucleotide variantNM_031212.4(SLC25A28):c.1006A>G (p.Ile336Val)not specified [RCV004291551]uncertain significance109961093899610938Humanname
405768022CV3325500single nucleotide variantNM_031212.4(SLC25A28):c.1025C>T (p.Ala342Val)not specified [RCV004456482]uncertain significance109961091999610919Humanname