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)

40 records found for search term Trmt12
Refine Term:
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156030361CV2202407single nucleotide variantNM_017956.4(TRMT12):c.65C>T (p.Ala22Val)not specified [RCV004080719]uncertain significance8124450992124450992Humanname
405759655CV3347484single nucleotide variantNM_017956.4(TRMT12):c.83G>C (p.Trp28Ser)not specified [RCV004468393]uncertain significance8124451010124451010Humanname
597679161CV3621726single nucleotide variantNM_017956.4(TRMT12):c.41G>A (p.Ser14Asn)not specified [RCV004883276]uncertain significance8124450968124450968Humanname
156190452CV2391112single nucleotide variantNM_017956.4(TRMT12):c.269C>T (p.Pro90Leu)not specified [RCV004235094]likely benign8124451196124451196Humanname
407454266CV3490855single nucleotide variantNM_017956.4(TRMT12):c.244A>T (p.Ser82Cys)not specified [RCV004684960]uncertain significance8124451171124451171Humanname
407461664CV3490856single nucleotide variantNM_017956.4(TRMT12):c.281C>T (p.Pro94Leu)not specified [RCV004687708]uncertain significance8124451208124451208Humanname
597678543CV3621722single nucleotide variantNM_017956.4(TRMT12):c.100A>G (p.Arg34Gly)not specified [RCV004883272]uncertain significance8124451027124451027Humanname
597679140CV3621728single nucleotide variantNM_017956.4(TRMT12):c.116G>A (p.Arg39Lys)not specified [RCV004883278]likely benign8124451043124451043Humanname
598214645CV3931955single nucleotide variantNM_017956.4(TRMT12):c.107A>G (p.Tyr36Cys)not specified [RCV005292571]uncertain significance8124451034124451034Humanname
598214654CV3931957single nucleotide variantNM_017956.4(TRMT12):c.227A>G (p.Asn76Ser)not specified [RCV005292573]uncertain significance8124451154124451154Humanname
156381221CV2218638single nucleotide variantNM_017956.4(TRMT12):c.541C>T (p.Pro181Ser)not specified [RCV004090893]uncertain significance8124451468124451468Humanname
156093757CV2252890single nucleotide variantNM_017956.4(TRMT12):c.824G>C (p.Arg275Thr)not specified [RCV004120722]uncertain significance8124451751124451751Humanname
156197448CV2259268single nucleotide variantNM_017956.4(TRMT12):c.856C>T (p.Arg286Trp)not specified [RCV004122288]uncertain significance8124451783124451783Humanname
156360658CV2269078single nucleotide variantNM_017956.4(TRMT12):c.302G>T (p.Cys101Phe)not specified [RCV004130257]uncertain significance8124451229124451229Humanname
155904951CV2349628single nucleotide variantNM_017956.4(TRMT12):c.802C>A (p.Pro268Thr)not specified [RCV004204049]uncertain significance8124451729124451729Humanname
156336909CV2360841single nucleotide variantNM_017956.4(TRMT12):c.571C>G (p.Leu191Val)not specified [RCV004213613]uncertain significance8124451498124451498Humanname
156342264CV2368524single nucleotide variantNM_017956.4(TRMT12):c.502C>T (p.Leu168Phe)not specified [RCV004221317]uncertain significance8124451429124451429Humanname
401737713CV2679955single nucleotide variantNM_017956.4(TRMT12):c.620G>A (p.Arg207His)not specified [RCV004284235]uncertain significance8124451547124451547Humanname
401872917CV2764424single nucleotide variantNM_017956.4(TRMT12):c.467T>C (p.Leu156Pro)not specified [RCV004338994]uncertain significance8124451394124451394Humanname
405759636CV3347481single nucleotide variantNM_017956.4(TRMT12):c.395G>T (p.Arg132Leu)not specified [RCV004468390]uncertain significance8124451322124451322Humanname
405759641CV3347482single nucleotide variantNM_017956.4(TRMT12):c.413G>A (p.Gly138Asp)not specified [RCV004468391]uncertain significance8124451340124451340Humanname
597678552CV3621723single nucleotide variantNM_017956.4(TRMT12):c.358G>T (p.Val120Phe)not specified [RCV004883273]uncertain significance8124451285124451285Humanname
597678562CV3621724single nucleotide variantNM_017956.4(TRMT12):c.382G>A (p.Ala128Thr)not specified [RCV004883274]uncertain significance8124451309124451309Humanname
597678570CV3621725single nucleotide variantNM_017956.4(TRMT12):c.391C>T (p.Pro131Ser)not specified [RCV004883275]uncertain significance8124451318124451318Humanname
597679150CV3621727single nucleotide variantNM_017956.4(TRMT12):c.338G>T (p.Arg113Leu)not specified [RCV004883277]uncertain significance8124451265124451265Humanname
597679121CV3621731single nucleotide variantNM_017956.4(TRMT12):c.560C>T (p.Pro187Leu)not specified [RCV004883280]uncertain significance8124451487124451487Humanname
597679111CV3621732single nucleotide variantNM_017956.4(TRMT12):c.672G>C (p.Glu224Asp)not specified [RCV004883281]uncertain significance8124451599124451599Humanname
598214650CV3931956single nucleotide variantNM_017956.4(TRMT12):c.375G>T (p.Glu125Asp)not specified [RCV005292572]uncertain significance8124451302124451302Humanname
156230593CV2199585single nucleotide variantNM_017956.4(TRMT12):c.1048C>T (p.Leu350Phe)not specified [RCV004072333]uncertain significance8124451975124451975Humanname
156018145CV2233028single nucleotide variantNM_017956.4(TRMT12):c.1219C>G (p.Leu407Val)not specified [RCV004103666]uncertain significance8124452146124452146Humanname
156160006CV2236292single nucleotide variantNM_017956.4(TRMT12):c.1292A>G (p.His431Arg)not specified [RCV004107989]uncertain significance8124452219124452219Humanname
156315287CV2250753single nucleotide variantNM_017956.4(TRMT12):c.1240C>T (p.Pro414Ser)not specified [RCV004129628]uncertain significance8124452167124452167Humanname
156335100CV2263660single nucleotide variantNM_017956.4(TRMT12):c.1271C>T (p.Pro424Leu)not specified [RCV004135660]uncertain significance8124452198124452198Humanname
156002154CV2287948single nucleotide variantNM_017956.4(TRMT12):c.1183T>C (p.Trp395Arg)not specified [RCV004147725]uncertain significance8124452110124452110Humanname
329356228CV2430644single nucleotide variantNM_017956.4(TRMT12):c.1283A>G (p.Tyr428Cys)not specified [RCV004253835]uncertain significance8124452210124452210Humanname
329377939CV2436084single nucleotide variantNM_017956.4(TRMT12):c.1045G>A (p.Ala349Thr)not specified [RCV004255300]uncertain significance8124451972124451972Humanname
405759624CV3347479single nucleotide variantNM_017956.4(TRMT12):c.1165A>G (p.Lys389Glu)not specified [RCV004468388]uncertain significance8124452092124452092Humanname
597678535CV3621721single nucleotide variantNM_017956.4(TRMT12):c.1321T>C (p.Cys441Arg)not specified [RCV004883271]uncertain significance8124452248124452248Humanname
597679131CV3621729single nucleotide variantNM_017956.4(TRMT12):c.1340T>C (p.Val447Ala)not specified [RCV004883279]uncertain significance8124452267124452267Humanname
598236340CV3931954single nucleotide variantNM_017956.4(TRMT12):c.1283A>C (p.Tyr428Ser)not specified [RCV005296006]uncertain significance8124452210124452210Humanname