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Variants search result for Homo sapiens
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43 records found for search term Gabrg1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8579902CV114304single nucleotide variantNM_173536.3(GABRG1):c.104+4643C>ALung cancer [RCV000094827]uncertain significance44611916746119167Humanname
9687146CV171377single nucleotide variantNM_173536.4(GABRG1):c.32C>T (p.Pro11Leu)Prostate cancer [RCV000149365]uncertain significance44612388246123882Human2name
405732476CV3254157single nucleotide variantNM_173536.4(GABRG1):c.37C>A (p.Leu13Ile)not specified [RCV004390164]uncertain significance44612387746123877Humanname
597743560CV3673318single nucleotide variantNM_173536.4(GABRG1):c.37C>T (p.Leu13Phe)not specified [RCV004922076]uncertain significance44612387746123877Humanname
617153935CV4022102duplicationNM_173536.4(GABRG1):c.161dup (p.Ala56fs)not provided [RCV005429156]not provided44609729246097293Humanname
15174437CV709374single nucleotide variantNM_173536.4(GABRG1):c.387C>T (p.Thr129=)not provided [RCV000972716]benign|likely benign44606551946065519Humanname
401757625CV2675422single nucleotide variantNM_173536.4(GABRG1):c.248T>C (p.Ile83Thr)not specified [RCV004292222]uncertain significance44609720646097206Humanname
405732440CV3254153single nucleotide variantNM_173536.4(GABRG1):c.129T>A (p.Asp43Glu)not specified [RCV004390160]uncertain significance44609732546097325Humanname
405732462CV3254155single nucleotide variantNM_173536.4(GABRG1):c.172A>G (p.Lys58Glu)not specified [RCV004390162]uncertain significance44609728246097282Humanname
407486234CV3439590single nucleotide variantNM_173536.4(GABRG1):c.190A>G (p.Ile64Val)not specified [RCV004619059]uncertain significance44609726446097264Humanname
407486241CV3439591single nucleotide variantNM_173536.4(GABRG1):c.184G>A (p.Gly62Arg)not specified [RCV004619060]uncertain significance44609727046097270Humanname
597743588CV3673324single nucleotide variantNM_173536.4(GABRG1):c.166G>A (p.Ala56Thr)not specified [RCV004922081]uncertain significance44609728846097288Humanname
598245311CV3977440single nucleotide variantNM_173536.4(GABRG1):c.249A>G (p.Ile83Met)not specified [RCV005344997]uncertain significance44609720546097205Humanname
8631185CV86341single nucleotide variantNM_173536.3(GABRG1):c.1341C>T (p.Phe447=)Malignant melanoma [RCV000066432]not provided44604104546041045Humanname
156151582CV2209292single nucleotide variantNM_173536.4(GABRG1):c.370T>G (p.Leu124Val)not specified [RCV004091691]uncertain significance44606553646065536Humanname
156046235CV2268671single nucleotide variantNM_173536.4(GABRG1):c.642T>G (p.Asn214Lys)not specified [RCV004124075]uncertain significance44605860646058606Humanname
156203471CV2313311single nucleotide variantNM_173536.4(GABRG1):c.372A>C (p.Leu124Phe)not specified [RCV004161553]uncertain significance44606553446065534Humanname
329367835CV2427583single nucleotide variantNM_173536.4(GABRG1):c.341T>A (p.Ile114Asn)not specified [RCV004250218]uncertain significance44606556546065565Humanname
329362077CV2456716single nucleotide variantNM_173536.4(GABRG1):c.589A>G (p.Met197Val)not specified [RCV004277882]uncertain significance44606447746064477Humanname
405732468CV3254156single nucleotide variantNM_173536.4(GABRG1):c.328A>G (p.Thr110Ala)not specified [RCV004390163]uncertain significance44606557846065578Humanname
597743578CV3673322single nucleotide variantNM_173536.4(GABRG1):c.782C>A (p.Thr261Lys)not specified [RCV004922079]uncertain significance44605835146058351Humanname
597743583CV3673323single nucleotide variantNM_173536.4(GABRG1):c.508A>G (p.Ile170Val)not specified [RCV004922080]uncertain significance44606539846065398Humanname
598245277CV3977436single nucleotide variantNM_173536.4(GABRG1):c.746T>C (p.Ile249Thr)not specified [RCV005344993]uncertain significance44605850246058502Humanname
598245286CV3977437single nucleotide variantNM_173536.4(GABRG1):c.947T>A (p.Leu316Gln)not specified [RCV005344994]uncertain significance44605160846051608Humanname
598245294CV3977438single nucleotide variantNM_173536.4(GABRG1):c.999G>A (p.Met333Ile)not specified [RCV005344995]uncertain significance44605155646051556Humanname
8631186CV86342single nucleotide variantNM_173536.3(GABRG1):c.660G>A (p.Trp220Ter)Malignant melanoma [RCV000066433]not provided44605858846058588Humanname
8631187CV86343single nucleotide variantNM_173536.3(GABRG1):c.390G>A (p.Met130Ile)Malignant melanoma [RCV000066434]not provided44606551646065516Humanname
8631188CV86344single nucleotide variantNM_173536.3(GABRG1):c.367C>T (p.Arg123Cys)Malignant melanoma [RCV000066435]not provided44606553946065539Humanname
156358764CV2260798single nucleotide variantNM_173536.4(GABRG1):c.1148A>G (p.His383Arg)not specified [RCV004125713]uncertain significance44604123846041238Humanname
156002734CV2288114single nucleotide variantNM_173536.4(GABRG1):c.1233T>G (p.Asp411Glu)not specified [RCV004149645]uncertain significance44604115346041153Humanname
156081618CV2301097single nucleotide variantNM_173536.4(GABRG1):c.1181T>C (p.Ile394Thr)not specified [RCV004158237]uncertain significance44604120546041205Humanname
156152232CV2318879single nucleotide variantNM_173536.4(GABRG1):c.1099A>G (p.Thr367Ala)not specified [RCV004175780]uncertain significance44605145646051456Humanname
156353885CV2324162single nucleotide variantNM_173536.4(GABRG1):c.1225G>T (p.Gly409Cys)not specified [RCV004176908]uncertain significance44604116146041161Humanname
329372750CV2434004single nucleotide variantNM_173536.4(GABRG1):c.1130C>T (p.Ser377Leu)not specified [RCV004249908]uncertain significance44605142546051425Humanname
329356970CV2460635single nucleotide variantNM_173536.4(GABRG1):c.1073C>T (p.Thr358Ile)not specified [RCV004270688]uncertain significance44605148246051482Humanname
401746770CV2731951single nucleotide variantNM_173536.4(GABRG1):c.1171A>G (p.Met391Val)not specified [RCV004333190]uncertain significance44604121546041215Humanname
401876635CV2767660single nucleotide variantNM_173536.4(GABRG1):c.1378G>A (p.Val460Ile)not specified [RCV004345800]uncertain significance44604100846041008Humanname
405732431CV3254152single nucleotide variantNM_173536.4(GABRG1):c.1265G>C (p.Cys422Ser)not specified [RCV004390159]uncertain significance44604112146041121Humanname
405732451CV3254154single nucleotide variantNM_173536.4(GABRG1):c.1335A>G (p.Ile445Met)not specified [RCV004390161]uncertain significance44604105146041051Humanname
597743566CV3673319single nucleotide variantNM_173536.4(GABRG1):c.1094C>T (p.Thr365Ile)not specified [RCV004922077]uncertain significance44605146146051461Humanname
597743572CV3673320single nucleotide variantNM_173536.4(GABRG1):c.1058C>T (p.Thr353Ile)not specified [RCV004922078]uncertain significance44605149746051497Humanname
597779455CV3673321single nucleotide variantNM_173536.4(GABRG1):c.1190C>T (p.Pro397Leu)not specified [RCV004930382]uncertain significance44604119646041196Humanname
598245303CV3977439single nucleotide variantNM_173536.4(GABRG1):c.1214A>T (p.Gln405Leu)not specified [RCV005344996]uncertain significance44604117246041172Humanname