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Variants search result for Homo sapiens
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67 records found for search term Pik3r6
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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