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47 records found for search term Hyal3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597783905CV3686295single nucleotide variantNM_003549.4(HYAL3):c.14T>C (p.Leu5Pro)not specified [RCV004931442]uncertain significance35029558950295589Humanname
156163637CV2389603single nucleotide variantNM_003549.4(HYAL3):c.85C>T (p.Arg29Cys)not specified [RCV004243665]uncertain significance35029551850295518Humanname
329354770CV2449020single nucleotide variantNM_003549.4(HYAL3):c.74A>G (p.Gln25Arg)not specified [RCV004264096]uncertain significance35029552950295529Humanname
401890674CV2775722single nucleotide variantNM_003549.4(HYAL3):c.82G>A (p.Glu28Lys)not specified [RCV004350849]uncertain significance35029552150295521Humanname
405781052CV3270781single nucleotide variantNM_003549.4(HYAL3):c.62A>G (p.Gln21Arg)not specified [RCV004397511]uncertain significance35029554150295541Humanname
156330329CV2210600single nucleotide variantNM_003549.4(HYAL3):c.134G>C (p.Arg45Pro)not specified [RCV004083751]uncertain significance35029546950295469Humanname
329382916CV2445671single nucleotide variantNM_003549.4(HYAL3):c.182G>A (p.Arg61His)not specified [RCV004259749]likely benign35029542150295421Humanname
405780367CV3270775single nucleotide variantNM_003549.4(HYAL3):c.134G>A (p.Arg45His)not specified [RCV004397505]uncertain significance35029546950295469Humanname
405781082CV3270776single nucleotide variantNM_003549.4(HYAL3):c.158A>G (p.Asn53Ser)not specified [RCV004397506]uncertain significance35029544550295445Humanname
597783897CV3686297single nucleotide variantNM_003549.4(HYAL3):c.272A>G (p.His91Arg)not specified [RCV004931444]uncertain significance35029533150295331Humanname
156397858CV2193837single nucleotide variantNM_003549.4(HYAL3):c.656G>A (p.Arg219His)not specified [RCV004074585]likely benign35029494750294947Humanname
156079689CV2258069single nucleotide variantNM_003549.4(HYAL3):c.694C>T (p.His232Tyr)not specified [RCV004121471]uncertain significance35029490950294909Humanname
155978135CV2321360single nucleotide variantNM_003549.4(HYAL3):c.659G>A (p.Cys220Tyr)not specified [RCV004177361]uncertain significance35029494450294944Humanname
156355441CV2324488single nucleotide variantNM_003549.4(HYAL3):c.475G>T (p.Asp159Tyr)not specified [RCV004178970]uncertain significance35029512850295128Humanname
155921783CV2340511single nucleotide variantNM_003549.4(HYAL3):c.880A>G (p.Arg294Gly)not specified [RCV004197231]uncertain significance35029472350294723Humanname
156285043CV2360739single nucleotide variantNM_003549.4(HYAL3):c.709G>A (p.Ala237Thr)not specified [RCV004213525]uncertain significance35029489450294894Humanname
156309204CV2366543single nucleotide variantNM_003549.4(HYAL3):c.679C>T (p.Arg227Cys)not specified [RCV004208517]uncertain significance35029492450294924Humanname
156036692CV2374008single nucleotide variantNM_003549.4(HYAL3):c.946G>A (p.Val316Met)not specified [RCV004227136]uncertain significance35029367050293670Humanname
329356514CV2430787single nucleotide variantNM_003549.4(HYAL3):c.532C>T (p.Arg178Cys)not specified [RCV004253964]uncertain significance35029507150295071Humanname
401720482CV2673342single nucleotide variantNM_003549.4(HYAL3):c.428G>A (p.Arg143Gln)not specified [RCV004288327]likely benign35029517550295175Humanname
401753536CV2684975single nucleotide variantNM_003549.4(HYAL3):c.557G>T (p.Arg186Leu)not specified [RCV004296470]uncertain significance35029504650295046Humanname
401730671CV2711440single nucleotide variantNM_003549.4(HYAL3):c.425G>A (p.Arg142His)not specified [RCV004313186]uncertain significance35029517850295178Humanname
401774443CV2713464single nucleotide variantNM_003549.4(HYAL3):c.976A>T (p.Ser326Cys)not specified [RCV004319073]uncertain significance35029364050293640Humanname
401784182CV2721124single nucleotide variantNM_003549.4(HYAL3):c.527C>T (p.Ala176Val)not specified [RCV004330141]uncertain significance35029507650295076Humanname
401888726CV2754865single nucleotide variantNM_003549.4(HYAL3):c.557G>A (p.Arg186Gln)not specified [RCV004341340]uncertain significance35029504650295046Humanname
401893278CV2766388single nucleotide variantNM_003549.4(HYAL3):c.368C>T (p.Pro123Leu)not specified [RCV004342632]likely benign35029523550295235Humanname
405781073CV3270778single nucleotide variantNM_003549.4(HYAL3):c.401T>C (p.Leu134Pro)not specified [RCV004397508]uncertain significance35029520250295202Humanname
405781065CV3270779single nucleotide variantNM_003549.4(HYAL3):c.469T>C (p.Phe157Leu)not specified [RCV004397509]uncertain significance35029513450295134Humanname
405781058CV3270780single nucleotide variantNM_003549.4(HYAL3):c.560T>G (p.Val187Gly)not specified [RCV004397510]uncertain significance35029504350295043Humanname
405781045CV3270782single nucleotide variantNM_003549.4(HYAL3):c.695A>G (p.His232Arg)not specified [RCV004397512]uncertain significance35029490850294908Humanname
405781039CV3270783single nucleotide variantNM_003549.4(HYAL3):c.857G>A (p.Arg286His)not specified [RCV004397513]uncertain significance35029474650294746Humanname
407465467CV3444284single nucleotide variantNM_003549.4(HYAL3):c.961G>A (p.Asp321Asn)not specified [RCV004635380]uncertain significance35029365550293655Humanname
407465470CV3444285single nucleotide variantNM_003549.4(HYAL3):c.782G>A (p.Arg261Gln)not specified [RCV004635381]uncertain significance35029482150294821Humanname
407465475CV3444286single nucleotide variantNM_003549.4(HYAL3):c.541A>T (p.Met181Leu)not specified [RCV004635382]uncertain significance35029506250295062Humanname
407465479CV3444287single nucleotide variantNM_003549.4(HYAL3):c.802T>C (p.Phe268Leu)not specified [RCV004635383]uncertain significance35029480150294801Humanname
407465483CV3444288single nucleotide variantNM_003549.4(HYAL3):c.440C>T (p.Ala147Val)not specified [RCV004635384]uncertain significance35029516350295163Humanname
597783908CV3686294single nucleotide variantNM_003549.4(HYAL3):c.680G>A (p.Arg227His)not specified [RCV004931441]uncertain significance35029492350294923Humanname
597783882CV3686301single nucleotide variantNM_003549.4(HYAL3):c.877G>A (p.Gly293Arg)not specified [RCV004931448]uncertain significance35029472650294726Humanname
156398025CV2194132single nucleotide variantNM_003549.4(HYAL3):c.1153G>A (p.Gly385Ser)not specified [RCV004076886]uncertain significance35029334750293347Humanname
156195372CV2306638single nucleotide variantNM_003549.4(HYAL3):c.1106G>A (p.Arg369Gln)not specified [RCV004157235]uncertain significance35029339450293394Humanname
156069022CV2355745single nucleotide variantNM_003549.4(HYAL3):c.1118G>C (p.Gly373Ala)not specified [RCV004199104]uncertain significance35029338250293382Humanname
329362001CV2456634single nucleotide variantNM_003549.4(HYAL3):c.1179C>G (p.Phe393Leu)not specified [RCV004277821]uncertain significance35029332150293321Humanname
401868680CV2785387single nucleotide variantNM_003549.4(HYAL3):c.1237C>T (p.Pro413Ser)not specified [RCV004357128]uncertain significance35029326350293263Humanname
597783901CV3686296single nucleotide variantNM_003549.4(HYAL3):c.1109G>A (p.Arg370Gln)not specified [RCV004931443]likely benign35029339150293391Humanname
597783893CV3686298single nucleotide variantNM_003549.4(HYAL3):c.1079G>A (p.Arg360Gln)not specified [RCV004931445]likely benign35029342150293421Humanname
597783890CV3686299single nucleotide variantNM_003549.4(HYAL3):c.1042A>C (p.Asn348His)not specified [RCV004931446]uncertain significance35029345850293458Humanname
597783886CV3686300single nucleotide variantNM_003549.4(HYAL3):c.1147C>A (p.Pro383Thr)not specified [RCV004931447]uncertain significance35029335350293353Humanname