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)

67 records found for search term Pik3r6
Refine Term:
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8585567CV120154single nucleotide variantNM_001010855.3(PIK3R6):c.-92+1033G>CLung cancer [RCV000100674]uncertain significance1788664968866496Humanname
156377945CV2207595single nucleotide variantNM_001010855.4(PIK3R6):c.40G>A (p.Val14Met)not specified [RCV004090381]uncertain significance1788396718839671Humanname
405790973CV3372683single nucleotide variantNM_001010855.4(PIK3R6):c.76C>T (p.Pro26Ser)not specified [RCV004505935]uncertain significance1788396358839635Humanname
597767377CV3575954single nucleotide variantNM_001010855.4(PIK3R6):c.56G>A (p.Arg19Gln)not specified [RCV004850454]uncertain significance1788396558839655Humanname
156079389CV2226539single nucleotide variantNM_001010855.4(PIK3R6):c.209G>A (p.Arg70Gln)not specified [RCV004101800]uncertain significance1788378528837852Humanname
329385340CV2432089single nucleotide variantNM_001010855.4(PIK3R6):c.142G>A (p.Gly48Ser)not specified [RCV004249239]uncertain significance1788386118838611Humanname
407530786CV3463637single nucleotide variantNM_001010855.4(PIK3R6):c.166A>C (p.Ile56Leu)not specified [RCV004657236]uncertain significance1788385878838587Humanname
597767386CV3575960single nucleotide variantNM_001010855.4(PIK3R6):c.122A>G (p.Lys41Arg)not specified [RCV004850456]uncertain significance1788386318838631Humanname
597740850CV3575964single nucleotide variantNM_001010855.4(PIK3R6):c.169C>T (p.Leu57Phe)not specified [RCV004844581]uncertain significance1788385848838584Humanname
597740855CV3575965single nucleotide variantNM_001010855.4(PIK3R6):c.158T>C (p.Leu53Pro)not specified [RCV004844582]uncertain significance1788385958838595Humanname
156141323CV2212283single nucleotide variantNM_001010855.4(PIK3R6):c.688G>A (p.Val230Met)not specified [RCV004090945]uncertain significance1788330038833003Humanname
156364558CV2271946single nucleotide variantNM_001010855.4(PIK3R6):c.421G>A (p.Glu141Lys)not specified [RCV004124765]uncertain significance1788365878836587Humanname
155917924CV2332905single nucleotide variantNM_001010855.4(PIK3R6):c.332C>G (p.Pro111Arg)not specified [RCV004192163]uncertain significance1788368508836850Humanname
156100889CV2351672single nucleotide variantNM_001010855.4(PIK3R6):c.739C>T (p.His247Tyr)not specified [RCV004195382]uncertain significance1788329528832952Humanname
156153340CV2374837single nucleotide variantNM_001010855.4(PIK3R6):c.964C>A (p.Gln322Lys)not specified [RCV004227872]uncertain significance1788289168828916Humanname
329377408CV2435910single nucleotide variantNM_001010855.4(PIK3R6):c.994C>T (p.Arg332Trp)not specified [RCV004255138]uncertain significance1788288868828886Humanname
329371879CV2442932single nucleotide variantNM_001010855.4(PIK3R6):c.712A>G (p.Ser238Gly)not specified [RCV004253531]uncertain significance1788329798832979Humanname
329373471CV2452414single nucleotide variantNM_001010855.4(PIK3R6):c.316C>A (p.Leu106Met)not specified [RCV004273031]uncertain significance1788368668836866Humanname
401737091CV2679224single nucleotide variantNM_001010855.4(PIK3R6):c.745G>A (p.Glu249Lys)not specified [RCV004285778]uncertain significance1788329468832946Humanname
401749782CV2694748single nucleotide variantNM_001010855.4(PIK3R6):c.329C>T (p.Thr110Ile)not specified [RCV004298834]uncertain significance1788368538836853Humanname
401725650CV2697499single nucleotide variantNM_001010855.4(PIK3R6):c.932G>A (p.Arg311His)not specified [RCV004297888]uncertain significance1788289488828948Humanname
401762849CV2710344single nucleotide variantNM_001010855.4(PIK3R6):c.981C>A (p.Asp327Glu)not specified [RCV004317514]uncertain significance1788288998828899Humanname
401771608CV2711786single nucleotide variantNM_001010855.4(PIK3R6):c.874G>A (p.Gly292Ser)not specified [RCV004309433]uncertain significance1788297218829721Humanname
401868923CV2767378single nucleotide variantNM_001010855.4(PIK3R6):c.784G>T (p.Ala262Ser)not specified [RCV004349538]uncertain significance1788329078832907Humanname
405790966CV3372681single nucleotide variantNM_001010855.4(PIK3R6):c.568C>T (p.Arg190Cys)not specified [RCV004505933]uncertain significance1788353508835350Humanname
405790970CV3372682single nucleotide variantNM_001010855.4(PIK3R6):c.596C>T (p.Ala199Val)not specified [RCV004505934]uncertain significance1788353228835322Humanname
405791253CV3372684single nucleotide variantNM_001010855.4(PIK3R6):c.821G>A (p.Arg274Gln)not specified [RCV004505936]uncertain significance1788297748829774Humanname
405790980CV3372685single nucleotide variantNM_001010855.4(PIK3R6):c.983G>A (p.Arg328Gln)not specified [RCV004505937]uncertain significance1788288978828897Humanname
407512082CV3463635single nucleotide variantNM_001010855.4(PIK3R6):c.653C>T (p.Pro218Leu)not specified [RCV004648272]uncertain significance1788330388833038Humanname
597740820CV3575955single nucleotide variantNM_001010855.4(PIK3R6):c.674A>G (p.Tyr225Cys)not specified [RCV004844574]uncertain significance1788330178833017Humanname
597740824CV3575956single nucleotide variantNM_001010855.4(PIK3R6):c.794G>A (p.Arg265His)not specified [RCV004844575]uncertain significance1788328978832897Humanname
597740832CV3575959single nucleotide variantNM_001010855.4(PIK3R6):c.731G>A (p.Arg244Gln)not specified [RCV004844577]uncertain significance1788329608832960Humanname
597740837CV3575961single nucleotide variantNM_001010855.4(PIK3R6):c.931C>T (p.Arg311Cys)not specified [RCV004844578]uncertain significance1788289498828949Humanname
598272782CV4006707single nucleotide variantNM_001010855.4(PIK3R6):c.569G>A (p.Arg190His)not specified [RCV005389478]uncertain significance1788353498835349Humanname
598272788CV4006708single nucleotide variantNM_001010855.4(PIK3R6):c.725C>A (p.Pro242Gln)not specified [RCV005389479]uncertain significance1788329668832966Humanname
598272791CV4006709single nucleotide variantNM_001010855.4(PIK3R6):c.709G>A (p.Ala237Thr)not specified [RCV005389480]uncertain significance1788329828832982Humanname
598272799CV4006711single nucleotide variantNM_001010855.4(PIK3R6):c.479A>G (p.Asp160Gly)not specified [RCV005389482]uncertain significance1788354398835439Humanname
598272804CV4006712single nucleotide variantNM_001010855.4(PIK3R6):c.485A>G (p.Glu162Gly)not specified [RCV005389483]uncertain significance1788354338835433Humanname
156140335CV2212167single nucleotide variantNM_001010855.4(PIK3R6):c.1756C>T (p.Pro586Ser)not specified [RCV004089065]uncertain significance1788226198822619Humanname
156117225CV2231837single nucleotide variantNM_001010855.4(PIK3R6):c.1012A>G (p.Thr338Ala)not specified [RCV004098639]uncertain significance1788288688828868Humanname
156172193CV2247499single nucleotide variantNM_001010855.4(PIK3R6):c.1264G>A (p.Gly422Arg)not specified [RCV004108818]uncertain significance1788286168828616Humanname
156303221CV2308246single nucleotide variantNM_001010855.4(PIK3R6):c.1945A>G (p.Asn649Asp)not specified [RCV004164744]uncertain significance1788191338819133Humanname
156361718CV2326685single nucleotide variantNM_001010855.4(PIK3R6):c.2040C>A (p.Ser680Arg)not specified [RCV004185263]uncertain significance1788041098804109Humanname
156174026CV2333761single nucleotide variantNM_001010855.4(PIK3R6):c.1583G>A (p.Arg528His)not specified [RCV004181269]uncertain significance1788234308823430Humanname
156183996CV2349882single nucleotide variantNM_001010855.4(PIK3R6):c.1199C>G (p.Pro400Arg)not specified [RCV004206303]uncertain significance1788286818828681Humanname
156056143CV2371015single nucleotide variantNM_001010855.4(PIK3R6):c.1450G>A (p.Val484Ile)not specified [RCV004220782]uncertain significance1788272378827237Humanname
155952852CV2393845single nucleotide variantNM_001010855.4(PIK3R6):c.1811G>T (p.Arg604Leu)not specified [RCV004233672]uncertain significance1788219148821914Humanname
329372210CV2443060single nucleotide variantNM_001010855.4(PIK3R6):c.1474G>A (p.Val492Ile)not specified [RCV004253648]uncertain significance1788272138827213Humanname
329391390CV2452299single nucleotide variantNM_001010855.4(PIK3R6):c.1580T>A (p.Ile527Asn)not specified [RCV004278977]uncertain significance1788234338823433Humanname
329396886CV2459163single nucleotide variantNM_001010855.4(PIK3R6):c.1234C>T (p.Arg412Trp)not specified [RCV004272612]uncertain significance1788286468828646Humanname
401729404CV2690209single nucleotide variantNM_001010855.4(PIK3R6):c.1066C>T (p.Pro356Ser)not specified [RCV004302218]uncertain significance1788288148828814Humanname
401782623CV2697126single nucleotide variantNM_001010855.4(PIK3R6):c.1114A>G (p.Ile372Val)not specified [RCV004302122]uncertain significance1788287668828766Humanname
401783664CV2723818single nucleotide variantNM_001010855.4(PIK3R6):c.1600A>G (p.Ile534Val)not specified [RCV004325966]uncertain significance1788234138823413Humanname
401890207CV2758847single nucleotide variantNM_001010855.4(PIK3R6):c.1382T>G (p.Leu461Arg)not specified [RCV004339939]uncertain significance1788281228828122Humanname
405790953CV3372677single nucleotide variantNM_001010855.4(PIK3R6):c.1138G>T (p.Asp380Tyr)not specified [RCV004505929]uncertain significance1788287428828742Humanname
405790957CV3372678single nucleotide variantNM_001010855.4(PIK3R6):c.1226G>C (p.Gly409Ala)not specified [RCV004505930]uncertain significance1788286548828654Humanname
405790963CV3372680single nucleotide variantNM_001010855.4(PIK3R6):c.1754G>A (p.Gly585Asp)not specified [RCV004505932]uncertain significance1788226218822621Humanname
407530782CV3463634single nucleotide variantNM_001010855.4(PIK3R6):c.1193G>A (p.Gly398Asp)not specified [RCV004657234]uncertain significance1788286878828687Humanname
407530784CV3463636single nucleotide variantNM_001010855.4(PIK3R6):c.1324A>G (p.Thr442Ala)not specified [RCV004657235]uncertain significance1788281808828180Humanname
407530788CV3463638single nucleotide variantNM_001010855.4(PIK3R6):c.1223C>T (p.Pro408Leu)not specified [RCV004657237]uncertain significance1788286578828657Humanname
407530791CV3463639single nucleotide variantNM_001010855.4(PIK3R6):c.1136T>G (p.Leu379Arg)not specified [RCV004657238]uncertain significance1788287448828744Humanname
597767381CV3575957single nucleotide variantNM_001010855.4(PIK3R6):c.1102C>T (p.Arg368Cys)not specified [RCV004850455]uncertain significance1788287788828778Humanname
597740826CV3575958single nucleotide variantNM_001010855.4(PIK3R6):c.1031G>A (p.Arg344Gln)not specified [RCV004844576]uncertain significance1788288498828849Humanname
597740846CV3575963single nucleotide variantNM_001010855.4(PIK3R6):c.1301A>G (p.Tyr434Cys)not specified [RCV004844580]uncertain significance1788285798828579Humanname
598272775CV4006704single nucleotide variantNM_001010855.4(PIK3R6):c.1537C>T (p.Arg513Trp)not specified [RCV005389476]uncertain significance1788234768823476Humanname
598272779CV4006705single nucleotide variantNM_001010855.4(PIK3R6):c.1804C>T (p.Arg602Trp)not specified [RCV005389477]uncertain significance1788219218821921Humanname
598272794CV4006710single nucleotide variantNM_001010855.4(PIK3R6):c.1225G>C (p.Gly409Arg)not specified [RCV005389481]uncertain significance1788286558828655Humanname