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Variants search result for Homo sapiens
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37 records found for search term Gjd3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
596945060CV3546890single nucleotide variantNM_152219.4(GJD3):c.237C>A (p.Leu79=)Meniere disease [RCV004808512]likely benign174036357940363579Human1name
156179983CV2327705single nucleotide variantNM_152219.4(GJD3):c.97C>T (p.Arg33Cys)not specified [RCV004177274]uncertain significance174036371940363719Humanname
596945058CV3546889single nucleotide variantNM_152219.4(GJD3):c.522G>C (p.Pro174=)Meniere disease [RCV004808511]likely benign174036329440363294Human1name
597707315CV3681137single nucleotide variantNM_152219.4(GJD3):c.80T>C (p.Val27Ala)not specified [RCV004917081]uncertain significance174036373640363736Humanname
155934783CV2225396single nucleotide variantNM_152219.4(GJD3):c.230T>C (p.Phe77Ser)not specified [RCV004100808]uncertain significance174036358640363586Humanname
156246188CV2263708single nucleotide variantNM_152219.4(GJD3):c.161G>C (p.Cys54Ser)not specified [RCV004136000]uncertain significance174036365540363655Humanname
155986286CV2282536single nucleotide variantNM_152219.4(GJD3):c.266C>G (p.Pro89Arg)not specified [RCV004135110]uncertain significance174036355040363550Humanname
156089230CV2359352single nucleotide variantNM_152219.4(GJD3):c.289A>T (p.Met97Leu)not specified [RCV004212631]uncertain significance174036352740363527Humanname
329393064CV2449474single nucleotide variantNM_152219.4(GJD3):c.221A>C (p.His74Pro)not specified [RCV004268417]uncertain significance174036359540363595Humanname
401783111CV2716134single nucleotide variantNM_152219.4(GJD3):c.157G>C (p.Val53Leu)not specified [RCV004323373]uncertain significance174036365940363659Humanname
597759549CV3681133single nucleotide variantNM_152219.4(GJD3):c.136G>C (p.Glu46Gln)not specified [RCV004925528]uncertain significance174036368040363680Humanname
597759554CV3681134single nucleotide variantNM_152219.4(GJD3):c.202C>G (p.Arg68Gly)not specified [RCV004925529]uncertain significance174036361440363614Humanname
597759558CV3681138single nucleotide variantNM_152219.4(GJD3):c.124G>C (p.Gly42Arg)not specified [RCV004925530]uncertain significance174036369240363692Humanname
597707324CV3681139single nucleotide variantNM_152219.4(GJD3):c.160T>A (p.Cys54Ser)not specified [RCV004917082]uncertain significance174036365640363656Humanname
156040664CV2219497single nucleotide variantNM_152219.4(GJD3):c.823G>A (p.Glu275Lys)not specified [RCV004095254]uncertain significance174036299340362993Humanname
156230068CV2235023single nucleotide variantNM_152219.4(GJD3):c.685C>A (p.Arg229Ser)not specified [RCV004113210]uncertain significance174036313140363131Humanname
156239257CV2269121single nucleotide variantNM_152219.4(GJD3):c.536G>T (p.Cys179Phe)not specified [RCV004130295]uncertain significance174036328040363280Humanname
156065308CV2272492single nucleotide variantNM_152219.4(GJD3):c.391C>T (p.Arg131Cys)not specified [RCV004133405]uncertain significance174036342540363425Humanname
156200729CV2362974single nucleotide variantNM_152219.4(GJD3):c.439G>A (p.Glu147Lys)not specified [RCV004211119]uncertain significance174036337740363377Humanname
155999245CV2378567single nucleotide variantNM_152219.4(GJD3):c.701C>T (p.Ala234Val)not specified [RCV004229003]uncertain significance174036311540363115Humanname
329376124CV2465227single nucleotide variantNM_152219.4(GJD3):c.718C>T (p.Pro240Ser)not specified [RCV004287260]uncertain significance174036309840363098Humanname
401899972CV2765882single nucleotide variantNM_152219.4(GJD3):c.491C>T (p.Pro164Leu)not specified [RCV004337917]uncertain significance174036332540363325Humanname
401880431CV2783207single nucleotide variantNM_152219.4(GJD3):c.632A>G (p.His211Arg)not specified [RCV004363547]uncertain significance174036318440363184Humanname
405737537CV3251554single nucleotide variantNM_152219.4(GJD3):c.404G>A (p.Cys135Tyr)not specified [RCV004390829]uncertain significance174036341240363412Humanname
405752167CV3251556single nucleotide variantNM_152219.4(GJD3):c.560A>C (p.Lys187Thr)not specified [RCV004392903]uncertain significance174036325640363256Humanname
405752173CV3251557single nucleotide variantNM_152219.4(GJD3):c.581A>G (p.Tyr194Cys)not specified [RCV004392904]uncertain significance174036323540363235Humanname
405752179CV3251558single nucleotide variantNM_152219.4(GJD3):c.635T>C (p.Leu212Pro)not specified [RCV004392905]uncertain significance174036318140363181Humanname
407513322CV3443279single nucleotide variantNM_152219.4(GJD3):c.398G>T (p.Arg133Leu)not specified [RCV004627143]uncertain significance174036341840363418Humanname
407513324CV3443280single nucleotide variantNM_152219.4(GJD3):c.751C>A (p.Pro251Thr)not specified [RCV004627144]uncertain significance174036306540363065Humanname
596945055CV3546887single nucleotide variantNM_152219.4(GJD3):c.758G>C (p.Arg253Pro)Meniere disease [RCV004808509]likely benign174036305840363058Human1name
596945057CV3546888single nucleotide variantNM_152219.4(GJD3):c.523C>T (p.His175Tyr)Meniere disease [RCV004808510]likely benign174036329340363293Human1name
597707304CV3681135single nucleotide variantNM_152219.4(GJD3):c.820C>T (p.Arg274Cys)not specified [RCV004917080]uncertain significance174036299640362996Humanname
597707334CV3681140single nucleotide variantNM_152219.4(GJD3):c.836G>T (p.Gly279Val)not specified [RCV004917083]uncertain significance174036298040362980Humanname
597707343CV3681141single nucleotide variantNM_152219.4(GJD3):c.436G>C (p.Ala146Pro)not specified [RCV004917084]uncertain significance174036338040363380Humanname
598251897CV3977739single nucleotide variantNM_152219.4(GJD3):c.655C>A (p.Arg219Ser)not specified [RCV005345992]uncertain significance174036316140363161Humanname
598251903CV3977740single nucleotide variantNM_152219.4(GJD3):c.787C>T (p.Pro263Ser)not specified [RCV005345993]uncertain significance174036302940363029Humanname
598251908CV3977741single nucleotide variantNM_152219.4(GJD3):c.400C>G (p.Arg134Gly)not specified [RCV005345994]uncertain significance174036341640363416Humanname