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40 records found for search term Rpusd3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156261851CV2319747single nucleotide variantNM_173659.5(RPUSD3):c.6C>G (p.Asp2Glu)not specified [RCV004187282]uncertain significance398439859843985Humanname
401871776CV2779393single nucleotide variantNM_173659.5(RPUSD3):c.23G>T (p.Gly8Val)not specified [RCV004351042]uncertain significance398439689843968Humanname
156263994CV2282622single nucleotide variantNM_173659.5(RPUSD3):c.46C>G (p.Arg16Gly)not specified [RCV004135181]uncertain significance398439459843945Humanname
329374012CV2447538single nucleotide variantNM_173659.5(RPUSD3):c.34A>G (p.Ser12Gly)not specified [RCV004255896]likely benign398439579843957Humanname
401732037CV2677979single nucleotide variantNM_173659.5(RPUSD3):c.59T>A (p.Val20Asp)not specified [RCV004296509]uncertain significance398439329843932Humanname
401730424CV2680312single nucleotide variantNM_173659.5(RPUSD3):c.40T>C (p.Trp14Arg)not specified [RCV004288565]uncertain significance398439519843951Humanname
407488352CV3476284single nucleotide variantNM_173659.5(RPUSD3):c.62G>A (p.Arg21His)not specified [RCV004665853]uncertain significance398439299843929Humanname
597710377CV3604444single nucleotide variantNM_173659.5(RPUSD3):c.73G>A (p.Glu25Lys)not specified [RCV004860950]uncertain significance398439189843918Humanname
329393212CV2449564single nucleotide variantNM_173659.5(RPUSD3):c.251C>T (p.Thr84Met)not specified [RCV004268494]uncertain significance398422319842231Humanname
405739977CV3316517single nucleotide variantNM_173659.5(RPUSD3):c.235A>G (p.Lys79Glu)not specified [RCV004452228]uncertain significance398434689843468Humanname
597786448CV3604440single nucleotide variantNM_173659.5(RPUSD3):c.202G>A (p.Val68Ile)not specified [RCV004854982]uncertain significance398435019843501Humanname
598221878CV3903105single nucleotide variantNM_173659.5(RPUSD3):c.203T>A (p.Val68Asp)not specified [RCV005272544]uncertain significance398435009843500Humanname
598221846CV3903111single nucleotide variantNM_173659.5(RPUSD3):c.220G>A (p.Ala74Thr)not specified [RCV005272550]uncertain significance398434839843483Humanname
598221832CV3903114single nucleotide variantNM_173659.5(RPUSD3):c.119G>A (p.Arg40His)not specified [RCV005272553]uncertain significance398435849843584Humanname
156079204CV2198365single nucleotide variantNM_173659.5(RPUSD3):c.626A>G (p.Lys209Arg)not specified [RCV004081908]uncertain significance398402589840258Humanname
156064265CV2240213single nucleotide variantNM_173659.5(RPUSD3):c.371G>T (p.Arg124Leu)not specified [RCV004112788]uncertain significance398419959841995Humanname
156121365CV2240819single nucleotide variantNM_173659.5(RPUSD3):c.863G>A (p.Arg288Lys)not specified [RCV004102114]uncertain significance398381859838185Humanname
155998437CV2260976single nucleotide variantNM_173659.5(RPUSD3):c.320C>T (p.Pro107Leu)not specified [RCV004125855]uncertain significance398420469842046Humanname
156157202CV2262383single nucleotide variantNM_173659.5(RPUSD3):c.814G>T (p.Ala272Ser)not specified [RCV004128832]uncertain significance398390589839058Humanname
11060094CV226898single nucleotide variantNM_173659.5(RPUSD3):c.724C>T (p.His242Tyr)Inborn genetic diseases [RCV000210730]likely pathogenic398391489839148Human1name
11060093CV226899single nucleotide variantNM_173659.5(RPUSD3):c.646C>T (p.Arg216Cys)Inborn genetic diseases [RCV000210726]likely pathogenic398402389840238Human1name
155978673CV2335135single nucleotide variantNM_173659.5(RPUSD3):c.784A>G (p.Thr262Ala)not specified [RCV004184666]uncertain significance398390889839088Humanname
329360530CV2458815single nucleotide variantNM_173659.5(RPUSD3):c.892G>A (p.Ala298Thr)not specified [RCV004270237]uncertain significance398381569838156Humanname
401719752CV2675674single nucleotide variantNM_173659.5(RPUSD3):c.865C>T (p.Arg289Cys)not specified [RCV004287925]uncertain significance398381839838183Humanname
401772222CV2719574single nucleotide variantNM_173659.5(RPUSD3):c.434G>A (p.Arg145His)not specified [RCV004327251]uncertain significance398407559840755Humanname
405739982CV3316518single nucleotide variantNM_173659.5(RPUSD3):c.302C>T (p.Thr101Met)not specified [RCV004452229]uncertain significance398420649842064Humanname
405739995CV3316520single nucleotide variantNM_173659.5(RPUSD3):c.796C>A (p.Gln266Lys)not specified [RCV004452231]uncertain significance398390769839076Humanname
407488359CV3476285single nucleotide variantNM_173659.5(RPUSD3):c.313G>C (p.Val105Leu)not specified [RCV004665854]uncertain significance398420539842053Humanname
407488366CV3476286single nucleotide variantNM_173659.5(RPUSD3):c.920A>G (p.His307Arg)not specified [RCV004665855]uncertain significance398381289838128Humanname
407513845CV3476287single nucleotide variantNM_173659.5(RPUSD3):c.661G>A (p.Gly221Ser)not specified [RCV004674268]uncertain significance398402239840223Humanname
597786452CV3604441single nucleotide variantNM_173659.5(RPUSD3):c.353A>C (p.Gln118Pro)not specified [RCV004854983]uncertain significance398420139842013Humanname
597786456CV3604442single nucleotide variantNM_173659.5(RPUSD3):c.607G>C (p.Asp203His)not specified [RCV004854984]uncertain significance398402779840277Humanname
597710369CV3604443single nucleotide variantNM_173659.5(RPUSD3):c.531G>C (p.Lys177Asn)not specified [RCV004860949]uncertain significance398405779840577Humanname
598221882CV3903104single nucleotide variantNM_173659.5(RPUSD3):c.776G>A (p.Arg259His)not specified [RCV005272543]uncertain significance398390969839096Humanname
598221873CV3903106single nucleotide variantNM_173659.5(RPUSD3):c.907C>T (p.His303Tyr)not specified [RCV005272545]uncertain significance398381419838141Humanname
598221868CV3903107single nucleotide variantNM_173659.5(RPUSD3):c.377C>G (p.Ser126Cys)not specified [RCV005272546]uncertain significance398419899841989Humanname
598221863CV3903108single nucleotide variantNM_173659.5(RPUSD3):c.765G>A (p.Met255Ile)not specified [RCV005272547]uncertain significance398391079839107Humanname
598221857CV3903109single nucleotide variantNM_173659.5(RPUSD3):c.623T>A (p.Val208Asp)not specified [RCV005272548]uncertain significance398402619840261Humanname
598221852CV3903110single nucleotide variantNM_173659.5(RPUSD3):c.740T>C (p.Leu247Pro)not specified [RCV005272549]uncertain significance398391329839132Humanname
156086563CV2340711single nucleotide variantNM_173659.5(RPUSD3):c.1021C>T (p.Arg341Cys)not specified [RCV004190382]likely benign398380279838027Humanname