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64 records found for search term Tprg1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8578482CV112865single nucleotide variantNM_198485.3(TPRG1):c.479+19067G>ALung cancer [RCV000093388]uncertain significance3189257976189257976Humanname
8630728CV85883single nucleotide variantNM_198485.3(TPRG1):c.231C>A (p.Ala77=)Malignant melanoma [RCV000065967]not provided3189215312189215312Humanname
155999620CV2287291single nucleotide variantNM_198485.4(TPRG1):c.89C>T (p.Ser30Leu)not specified [RCV004146924]uncertain significance3189207473189207473Humanname
405775004CV3343917single nucleotide variantNM_198485.4(TPRG1):c.61G>A (p.Asp21Asn)not specified [RCV004470953]uncertain significance3189207445189207445Humanname
598201171CV3928393single nucleotide variantNM_198485.4(TPRG1):c.59A>T (p.Asp20Val)not specified [RCV005290119]uncertain significance3189207443189207443Humanname
155964304CV2282826single nucleotide variantNM_198485.4(TPRG1):c.259G>C (p.Glu87Gln)not specified [RCV004143487]uncertain significance3189215340189215340Humanname
156196535CV2347739single nucleotide variantNM_198485.4(TPRG1):c.191G>A (p.Arg64Gln)not specified [RCV004202706]uncertain significance3189207575189207575Humanname
155933337CV2372258single nucleotide variantNM_198485.4(TPRG1):c.182A>C (p.Tyr61Ser)not specified [RCV004217036]uncertain significance3189207566189207566Humanname
329371589CV2458911single nucleotide variantNM_198485.4(TPRG1):c.292C>T (p.Leu98Phe)not specified [RCV004270318]uncertain significance3189215373189215373Humanname
401741625CV2676489single nucleotide variantNM_198485.4(TPRG1):c.190C>T (p.Arg64Trp)not specified [RCV004288688]uncertain significance3189207574189207574Humanname
401723424CV2724896single nucleotide variantNM_198485.4(TPRG1):c.283G>A (p.Gly95Ser)not specified [RCV004319671]uncertain significance3189215364189215364Humanname
405774986CV3343914single nucleotide variantNM_198485.4(TPRG1):c.143C>T (p.Thr48Ile)not specified [RCV004470950]uncertain significance3189207527189207527Humanname
405774992CV3343915single nucleotide variantNM_198485.4(TPRG1):c.278T>C (p.Ile93Thr)not specified [RCV004470951]uncertain significance3189215359189215359Humanname
407521525CV3492418single nucleotide variantNM_198485.4(TPRG1):c.253G>A (p.Val85Ile)not specified [RCV004677342]likely benign3189215334189215334Humanname
407521528CV3492419single nucleotide variantNM_198485.4(TPRG1):c.186C>G (p.Ile62Met)not specified [RCV004677343]uncertain significance3189207570189207570Humanname
597795589CV3620868single nucleotide variantNM_198485.4(TPRG1):c.145G>A (p.Glu49Lys)not specified [RCV004878234]uncertain significance3189207529189207529Humanname
156156764CV2238553single nucleotide variantNM_198485.4(TPRG1):c.365T>C (p.Ile122Thr)not specified [RCV004107167]uncertain significance3189238795189238795Humanname
156258781CV2277774single nucleotide variantNM_198485.4(TPRG1):c.805G>T (p.Ala269Ser)not specified [RCV004147206]uncertain significance3189320797189320797Humanname
156202056CV2300600single nucleotide variantNM_198485.4(TPRG1):c.525G>T (p.Glu175Asp)not specified [RCV004155559]uncertain significance3189310431189310431Humanname
156204341CV2331656single nucleotide variantNM_198485.4(TPRG1):c.595A>G (p.Met199Val)not specified [RCV004184286]uncertain significance3189310501189310501Humanname
156392141CV2378315single nucleotide variantNM_198485.4(TPRG1):c.424G>A (p.Ala142Thr)not specified [RCV004226344]uncertain significance3189238854189238854Humanname
155992912CV2381638single nucleotide variantNM_198485.4(TPRG1):c.809G>A (p.Arg270His)not specified [RCV004232109]uncertain significance3189320801189320801Humanname
156053088CV2385473single nucleotide variantNM_198485.4(TPRG1):c.781C>T (p.Arg261Cys)not specified [RCV004233120]uncertain significance3189320773189320773Humanname
401724953CV2697224single nucleotide variantNM_198485.4(TPRG1):c.484C>G (p.Gln162Glu)not specified [RCV004303998]uncertain significance3189310390189310390Humanname
401767606CV2727218single nucleotide variantNM_198485.4(TPRG1):c.667A>C (p.Ile223Leu)not specified [RCV004327348]uncertain significance3189320659189320659Humanname
401890350CV2755811single nucleotide variantNM_198485.4(TPRG1):c.434G>C (p.Arg145Pro)not specified [RCV004342183]uncertain significance3189238864189238864Humanname
401865026CV2768642single nucleotide variantNM_198485.4(TPRG1):c.494G>A (p.Gly165Asp)not specified [RCV004344494]uncertain significance3189310400189310400Humanname
401869663CV2772480single nucleotide variantNM_198485.4(TPRG1):c.484C>A (p.Gln162Lys)not specified [RCV004355259]uncertain significance3189310390189310390Humanname
597795581CV3620865single nucleotide variantNM_198485.4(TPRG1):c.808C>T (p.Arg270Cys)not specified [RCV004878231]uncertain significance3189320800189320800Humanname
597795583CV3620866single nucleotide variantNM_198485.4(TPRG1):c.359T>C (p.Leu120Pro)not specified [RCV004878232]uncertain significance3189238789189238789Humanname
597795586CV3620867single nucleotide variantNM_198485.4(TPRG1):c.481A>G (p.Arg161Gly)not specified [RCV004878233]uncertain significance3189310387189310387Humanname
597795593CV3620869single nucleotide variantNM_198485.4(TPRG1):c.515G>A (p.Ser172Asn)not specified [RCV004878235]uncertain significance3189310421189310421Humanname
597795597CV3620870single nucleotide variantNM_198485.4(TPRG1):c.577A>G (p.Thr193Ala)not specified [RCV004878236]uncertain significance3189310483189310483Humanname
597795601CV3620871single nucleotide variantNM_198485.4(TPRG1):c.415C>A (p.Pro139Thr)not specified [RCV004878237]uncertain significance3189238845189238845Humanname
597795604CV3620872single nucleotide variantNM_198485.4(TPRG1):c.766T>A (p.Ser256Thr)not specified [RCV004878238]uncertain significance3189320758189320758Humanname
598265122CV3928394single nucleotide variantNM_198485.4(TPRG1):c.502A>T (p.Ile168Phe)not specified [RCV005281033]uncertain significance3189310408189310408Humanname
156228975CV2234936single nucleotide variantNM_182752.4(TPRG1L):c.16G>T (p.Asp6Tyr)not specified [RCV004113139]uncertain significance136250883625088Humanname
405775016CV3343919single nucleotide variantNM_182752.4(TPRG1L):c.19T>G (p.Ser7Ala)not specified [RCV004470955]uncertain significance136250913625091Humanname
598201195CV3928399single nucleotide variantNM_182752.4(TPRG1L):c.23T>G (p.Val8Gly)not specified [RCV005290123]uncertain significance136250953625095Humanname
405775028CV3343921single nucleotide variantNM_182752.4(TPRG1L):c.85G>T (p.Gly29Cys)not specified [RCV004470957]uncertain significance136251573625157Humanname
597795620CV3620877single nucleotide variantNM_182752.4(TPRG1L):c.97G>C (p.Gly33Arg)not specified [RCV004878243]uncertain significance136251693625169Humanname
598201176CV3928396single nucleotide variantNM_182752.4(TPRG1L):c.41G>A (p.Ser14Asn)not specified [RCV005290120]uncertain significance136251133625113Humanname
156172589CV2286934single nucleotide variantNM_182752.4(TPRG1L):c.127C>T (p.Arg43Cys)not specified [RCV004144540]uncertain significance136251993625199Humanname
156286358CV2292076single nucleotide variantNM_182752.4(TPRG1L):c.112G>A (p.Ala38Thr)not specified [RCV004160348]likely benign136251843625184Humanname
156272901CV2320144single nucleotide variantNM_182752.4(TPRG1L):c.182A>G (p.Lys61Arg)not specified [RCV004167985]uncertain significance136252543625254Humanname
407521530CV3492420single nucleotide variantNM_182752.4(TPRG1L):c.122C>T (p.Pro41Leu)not specified [RCV004677344]uncertain significance136251943625194Humanname
597795607CV3620873single nucleotide variantNM_182752.4(TPRG1L):c.113C>T (p.Ala38Val)not specified [RCV004878239]uncertain significance136251853625185Humanname
597795617CV3620876single nucleotide variantNM_182752.4(TPRG1L):c.199C>G (p.Arg67Gly)not specified [RCV004878242]uncertain significance136252713625271Humanname
598201183CV3928397single nucleotide variantNM_182752.4(TPRG1L):c.205G>A (p.Gly69Ser)not specified [RCV005290121]uncertain significance136254273625427Humanname
156169666CV2197810single nucleotide variantNM_182752.4(TPRG1L):c.556G>A (p.Val186Met)not specified [RCV004077049]uncertain significance136275853627585Humanname
156399994CV2202350single nucleotide variantNM_182752.4(TPRG1L):c.510A>T (p.Gln170His)not specified [RCV004078274]uncertain significance136275393627539Humanname
156242738CV2210760single nucleotide variantNM_182752.4(TPRG1L):c.535T>C (p.Trp179Arg)not specified [RCV004085856]uncertain significance136275643627564Humanname
155910770CV2303672single nucleotide variantNM_182752.4(TPRG1L):c.341A>T (p.Glu114Val)not specified [RCV004161745]uncertain significance136257603625760Humanname
156359913CV2328333single nucleotide variantNM_182752.4(TPRG1L):c.413A>G (p.Asn138Ser)not specified [RCV004175450]likely benign136258323625832Humanname
156215770CV2347901single nucleotide variantNM_182752.4(TPRG1L):c.431C>T (p.Ser144Phe)not specified [RCV004197595]uncertain significance136258503625850Humanname
156007188CV2394330single nucleotide variantNM_182752.4(TPRG1L):c.754A>T (p.Met252Leu)not specified [RCV004238550]uncertain significance136285383628538Humanname
329396053CV2463207single nucleotide variantNM_182752.4(TPRG1L):c.550A>G (p.Thr184Ala)not specified [RCV004274984]uncertain significance136275793627579Humanname
401759822CV2707159single nucleotide variantNM_182752.4(TPRG1L):c.721C>T (p.Arg241Cys)not specified [RCV004315523]uncertain significance136285053628505Humanname
401872436CV2779656single nucleotide variantNM_182752.4(TPRG1L):c.722G>A (p.Arg241His)not specified [RCV004351352]uncertain significance136285063628506Humanname
405775022CV3343920single nucleotide variantNM_182752.4(TPRG1L):c.338C>T (p.Thr113Met)not specified [RCV004470956]uncertain significance136257573625757Humanname
407461237CV3492421single nucleotide variantNM_182752.4(TPRG1L):c.554A>C (p.Asn185Thr)not specified [RCV004687603]uncertain significance136275833627583Humanname
597795623CV3620878single nucleotide variantNM_182752.4(TPRG1L):c.545G>C (p.Trp182Ser)not specified [RCV004878244]uncertain significance136275743627574Humanname
598265126CV3928395single nucleotide variantNM_182752.4(TPRG1L):c.467A>G (p.Asn156Ser)not specified [RCV005281034]uncertain significance136258863625886Humanname
598201189CV3928398single nucleotide variantNM_182752.4(TPRG1L):c.724C>G (p.Pro242Ala)not specified [RCV005290122]uncertain significance136285083628508Humanname