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Variants search result for Homo sapiens
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25 records found for search term Tmod3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156135538CV2196103single nucleotide variantNM_014547.5(TMOD3):c.17G>A (p.Arg6His)not specified [RCV004073467]uncertain significance155186290151862901Humanname
156112245CV2228423single nucleotide variantNM_014547.5(TMOD3):c.74C>T (p.Ser25Leu)not specified [RCV004098398]uncertain significance155186295851862958Humanname
597801021CV3610842single nucleotide variantNM_014547.5(TMOD3):c.62T>C (p.Leu21Pro)not specified [RCV004880462]uncertain significance155186294651862946Humanname
155969926CV2400820single nucleotide variantNM_014547.5(TMOD3):c.181A>G (p.Thr61Ala)not specified [RCV004242477]uncertain significance155186927151869271Humanname
329377167CV2451892single nucleotide variantNM_014547.5(TMOD3):c.269C>G (p.Thr90Ser)not specified [RCV004276565]uncertain significance155186935951869359Humanname
156300200CV2248776single nucleotide variantNM_014547.5(TMOD3):c.674C>G (p.Thr225Ser)not specified [RCV004121927]uncertain significance155189646551896465Humanname
156244152CV2283327single nucleotide variantNM_014547.5(TMOD3):c.463A>G (p.Ser155Gly)not specified [RCV004145986]uncertain significance155188911251889112Humanname
156299025CV2310684single nucleotide variantNM_014547.5(TMOD3):c.712C>T (p.Arg238Trp)not specified [RCV004157341]uncertain significance155189650351896503Humanname
156306247CV2314896single nucleotide variantNM_014547.5(TMOD3):c.895A>G (p.Thr299Ala)not specified [RCV004171009]uncertain significance155190190751901907Humanname
155970854CV2335626single nucleotide variantNM_014547.5(TMOD3):c.524C>T (p.Pro175Leu)not specified [RCV004193830]uncertain significance155189384251893842Humanname
156134916CV2347158single nucleotide variantNM_014547.5(TMOD3):c.536A>G (p.Glu179Gly)not specified [RCV004204634]uncertain significance155189385451893854Humanname
156208543CV2382520single nucleotide variantNM_014547.5(TMOD3):c.553A>G (p.Asn185Asp)not specified [RCV004232855]uncertain significance155189387151893871Humanname
329394180CV2472366single nucleotide variantNM_014547.5(TMOD3):c.685G>A (p.Val229Met)not specified [RCV004285246]uncertain significance155189647651896476Humanname
401892557CV2782201single nucleotide variantNM_014547.5(TMOD3):c.697A>G (p.Ser233Gly)not specified [RCV004359177]uncertain significance155189648851896488Humanname
405773185CV3343423single nucleotide variantNM_014547.5(TMOD3):c.532G>A (p.Asp178Asn)not specified [RCV004470650]uncertain significance155189385051893850Humanname
407527148CV3482919single nucleotide variantNM_014547.5(TMOD3):c.680C>T (p.Thr227Ile)not specified [RCV004679897]uncertain significance155189647151896471Humanname
407527151CV3482920single nucleotide variantNM_014547.5(TMOD3):c.407C>G (p.Ala136Gly)not specified [RCV004679898]uncertain significance155188905651889056Humanname
597801031CV3610837single nucleotide variantNM_014547.5(TMOD3):c.719A>G (p.Asn240Ser)not specified [RCV004880457]uncertain significance155189651051896510Humanname
597801030CV3610838single nucleotide variantNM_014547.5(TMOD3):c.550A>G (p.Thr184Ala)not specified [RCV004880458]uncertain significance155189386851893868Humanname
597801028CV3610839single nucleotide variantNM_014547.5(TMOD3):c.497A>G (p.Asn166Ser)not specified [RCV004880459]uncertain significance155189381551893815Humanname
597801024CV3610841single nucleotide variantNM_014547.5(TMOD3):c.637A>G (p.Ile213Val)not specified [RCV004880461]uncertain significance155189642851896428Humanname
598227998CV3914140single nucleotide variantNM_014547.5(TMOD3):c.310C>A (p.Pro104Thr)not specified [RCV005294675]uncertain significance155188761551887615Humanname
598252884CV3914141single nucleotide variantNM_014547.5(TMOD3):c.901G>A (p.Val301Ile)not specified [RCV005278157]uncertain significance155190191351901913Humanname
598228004CV3914142single nucleotide variantNM_014547.5(TMOD3):c.833C>T (p.Ala278Val)not specified [RCV005294676]uncertain significance155190025251900252Humanname
598228010CV3914143single nucleotide variantNM_014547.5(TMOD3):c.1039G>A (p.Val347Ile)not specified [RCV005294677]uncertain significance155190879051908790Humanname