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22 records found for search term Hes6
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405803270CV3273860single nucleotide variantNM_018645.6(HES6):c.63G>C (p.Glu21Asp)not specified [RCV004404356]uncertain significance2238239843238239843Humanname
407521804CV3437176single nucleotide variantNM_018645.6(HES6):c.65C>T (p.Thr22Met)not specified [RCV004630492]uncertain significance2238239841238239841Humanname
156083921CV2205549single nucleotide variantNM_018645.6(HES6):c.289G>A (p.Ala97Thr)not specified [RCV004082478]uncertain significance2238239213238239213Humanname
156083208CV2244456single nucleotide variantNM_018645.6(HES6):c.292G>A (p.Ala98Thr)not specified [RCV004100421]uncertain significance2238239210238239210Humanname
156280823CV2338420single nucleotide variantNM_018645.6(HES6):c.238G>A (p.Gly80Ser)not provided [RCV004695578]|not specified [RCV004186464]uncertain significance2238239499238239499Humanname
401861237CV2769596single nucleotide variantNM_018645.6(HES6):c.154C>G (p.Leu52Val)not specified [RCV004351241]uncertain significance2238239675238239675Humanname
597761159CV3685633single nucleotide variantNM_018645.6(HES6):c.193G>A (p.Glu65Lys)not specified [RCV004925846]uncertain significance2238239544238239544Humanname
156077906CV2248210single nucleotide variantNM_018645.6(HES6):c.511A>G (p.Ile171Val)not specified [RCV004117601]uncertain significance2238238991238238991Humanname
156185181CV2346498single nucleotide variantNM_018645.6(HES6):c.413G>A (p.Gly138Asp)not specified [RCV004206421]uncertain significance2238239089238239089Humanname
156097972CV2384993single nucleotide variantNM_018645.6(HES6):c.589C>T (p.Pro197Ser)not specified [RCV004228265]uncertain significance2238238913238238913Humanname
329362110CV2448305single nucleotide variantNM_018645.6(HES6):c.395C>T (p.Ser132Phe)not specified [RCV004256595]uncertain significance2238239107238239107Humanname
329371824CV2454908single nucleotide variantNM_018645.6(HES6):c.590C>T (p.Pro197Leu)not specified [RCV004270401]uncertain significance2238238912238238912Humanname
329377914CV2458965single nucleotide variantNM_018645.6(HES6):c.509C>T (p.Pro170Leu)not specified [RCV004272453]uncertain significance2238238993238238993Humanname
401894854CV2781915single nucleotide variantNM_018645.6(HES6):c.452G>A (p.Gly151Glu)not specified [RCV004357158]uncertain significance2238239050238239050Humanname
405803263CV3273856single nucleotide variantNM_018645.6(HES6):c.305A>G (p.Gln102Arg)not specified [RCV004404352]uncertain significance2238239197238239197Humanname
405803265CV3273857single nucleotide variantNM_018645.6(HES6):c.399G>A (p.Met133Ile)not specified [RCV004404353]uncertain significance2238239103238239103Humanname
405803266CV3273858single nucleotide variantNM_018645.6(HES6):c.449C>T (p.Ala150Val)not specified [RCV004404354]uncertain significance2238239053238239053Humanname
405803268CV3273859single nucleotide variantNM_018645.6(HES6):c.613C>T (p.Pro205Ser)not specified [RCV004404355]uncertain significance2238238889238238889Humanname
597761156CV3685632single nucleotide variantNM_018645.6(HES6):c.524C>T (p.Pro175Leu)not specified [RCV004925845]uncertain significance2238238978238238978Humanname
598177135CV3978660single nucleotide variantNM_018645.6(HES6):c.483G>C (p.Trp161Cys)not specified [RCV005351780]uncertain significance2238239019238239019Humanname
598177142CV3978661single nucleotide variantNM_018645.6(HES6):c.638C>G (p.Thr213Arg)not specified [RCV005351781]uncertain significance2238238864238238864Humanname
598177149CV3978662single nucleotide variantNM_018645.6(HES6):c.380A>G (p.Asn127Ser)not specified [RCV005351782]uncertain significance2238239122238239122Humanname