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Variants search result for All species
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38 records found for search term Allc
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401910844CV2815497single nucleotide variantNM_018436.4(ALLC):c.975+4C>Tnot provided [RCV003425490]likely benign237016403701640Humanname
156143913CV2383891single nucleotide variantNM_018436.4(ALLC):c.26G>C (p.Gly9Ala)not specified [RCV004231749]uncertain significance236711833671183Humanname
329377721CV2436013single nucleotide variantNM_018436.4(ALLC):c.19T>A (p.Ser7Thr)not specified [RCV004255233]uncertain significance236711763671176Humanname
401783307CV2716267single nucleotide variantNM_018436.4(ALLC):c.97T>C (p.Cys33Arg)not specified [RCV004323485]uncertain significance236784803678480Humanname
401888468CV2761460single nucleotide variantNM_018436.4(ALLC):c.95C>G (p.Pro32Arg)not specified [RCV004334635]uncertain significance236784783678478Humanname
405795104CV3275329single nucleotide variantNM_018436.4(ALLC):c.95C>A (p.Pro32Gln)not specified [RCV004401103]uncertain significance236784783678478Humanname
156274380CV2344230single nucleotide variantNM_018436.4(ALLC):c.217C>T (p.Arg73Trp)not specified [RCV004197866]uncertain significance236799133679913Humanname
156003332CV2396723single nucleotide variantNM_018436.4(ALLC):c.284C>A (p.Ala95Glu)not specified [RCV004233877]uncertain significance236799803679980Humanname
405794962CV3275279single nucleotide variantNM_018436.4(ALLC):c.239C>G (p.Ser80Cys)not specified [RCV004401053]uncertain significance236799353679935Humanname
407459683CV3451916single nucleotide variantNM_018436.4(ALLC):c.220G>A (p.Gly74Ser)not specified [RCV004633653]uncertain significance236799163679916Humanname
598255370CV3971351single nucleotide variantNM_018436.4(ALLC):c.150G>T (p.Glu50Asp)not specified [RCV005346543]uncertain significance236785333678533Humanname
598255462CV3971377single nucleotide variantNM_018436.4(ALLC):c.266G>C (p.Arg89Pro)not specified [RCV005346562]uncertain significance236799623679962Humanname
156147124CV2196932single nucleotide variantNM_018436.4(ALLC):c.938C>T (p.Pro313Leu)not specified [RCV004071394]uncertain significance237015993701599Humanname
156322905CV2205285single nucleotide variantNM_018436.4(ALLC):c.467A>G (p.Asn156Ser)not specified [RCV004079905]uncertain significance236830303683030Humanname
155925536CV2258558single nucleotide variantNM_018436.4(ALLC):c.513T>A (p.Asp171Glu)not specified [RCV004116039]uncertain significance236957183695718Humanname
156146529CV2289223single nucleotide variantNM_018436.4(ALLC):c.610G>A (p.Gly204Arg)not specified [RCV004152218]uncertain significance236958153695815Humanname
156226610CV2352762single nucleotide variantNM_018436.4(ALLC):c.724C>T (p.Arg242Trp)not specified [RCV004198779]uncertain significance236963313696331Humanname
156152948CV2367182single nucleotide variantNM_018436.4(ALLC):c.725G>A (p.Arg242Gln)not specified [RCV004215611]uncertain significance236963323696332Humanname
156270434CV2379507single nucleotide variantNM_018436.4(ALLC):c.436C>G (p.Pro146Ala)not specified [RCV004217222]uncertain significance236829993682999Humanname
401738671CV2676346single nucleotide variantNM_018436.4(ALLC):c.955C>G (p.Pro319Ala)not specified [RCV004286375]uncertain significance237016163701616Humanname
401729438CV2690232single nucleotide variantNM_018436.4(ALLC):c.721G>T (p.Asp241Tyr)not specified [RCV004302238]uncertain significance236963283696328Humanname
401882154CV2781495single nucleotide variantNM_018436.4(ALLC):c.737T>C (p.Leu246Ser)not specified [RCV004354728]uncertain significance236963443696344Humanname
405794990CV3275289single nucleotide variantNM_018436.4(ALLC):c.372T>G (p.Ile124Met)not specified [RCV004401063]uncertain significance236817073681707Humanname
405795023CV3275300single nucleotide variantNM_018436.4(ALLC):c.542G>T (p.Gly181Val)not specified [RCV004401074]uncertain significance236957473695747Humanname
405795061CV3275313single nucleotide variantNM_018436.4(ALLC):c.750G>C (p.Glu250Asp)not specified [RCV004401087]likely benign236973563697356Humanname
405795069CV3275316single nucleotide variantNM_018436.4(ALLC):c.804T>A (p.His268Gln)not specified [RCV004401090]uncertain significance236974103697410Humanname
407459579CV3451894single nucleotide variantNM_018436.4(ALLC):c.971C>T (p.Thr324Ile)not specified [RCV004633634]uncertain significance237016323701632Humanname
407459636CV3451905single nucleotide variantNM_018436.4(ALLC):c.461T>A (p.Leu154His)not specified [RCV004633644]uncertain significance236830243683024Humanname
597791609CV3679464single nucleotide variantNM_018436.4(ALLC):c.770C>T (p.Pro257Leu)not specified [RCV004933590]uncertain significance236973763697376Humanname
597791880CV3679482single nucleotide variantNM_018436.4(ALLC):c.646G>T (p.Gly216Trp)not specified [RCV004933606]uncertain significance236958513695851Humanname
598255444CV3971368single nucleotide variantNM_018436.4(ALLC):c.541G>T (p.Gly181Cys)not specified [RCV005346558]uncertain significance236957463695746Humanname
15115941CV708268single nucleotide variantNM_018436.4(ALLC):c.794G>A (p.Arg265Gln)not provided [RCV000961944]benign236974003697400Humanname
15115948CV708269single nucleotide variantNM_018436.4(ALLC):c.868T>C (p.Cys290Arg)not provided [RCV000961945]benign237015293701529Humanname
156001711CV2378845single nucleotide variantNM_018436.4(ALLC):c.1054A>G (p.Ile352Val)not specified [RCV004231287]uncertain significance237024413702441Humanname
401783714CV2723872single nucleotide variantNM_018436.4(ALLC):c.1012A>T (p.Thr338Ser)not specified [RCV004326009]uncertain significance237023993702399Humanname
405794936CV3275270single nucleotide variantNM_018436.4(ALLC):c.1121G>A (p.Arg374Lys)not specified [RCV004401044]uncertain significance237025083702508Humanname
597791680CV3679493single nucleotide variantNM_018436.4(ALLC):c.1099C>T (p.Pro367Ser)not specified [RCV004933614]uncertain significance237024863702486Humanname
598246336CV3971384single nucleotide variantNM_018436.4(ALLC):c.1088T>C (p.Leu363Pro)not specified [RCV005345140]uncertain significance237024753702475Humanname