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Variants search result for Homo sapiens
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21 records found for search term Hes3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405803242CV3273845single nucleotide variantNM_001024598.4(HES3):c.92G>A (p.Arg31His)not specified [RCV004404341]uncertain significance162445586244558Humanname
407521792CV3437170single nucleotide variantNM_001024598.4(HES3):c.86G>A (p.Arg29Gln)not specified [RCV004630488]likely benign162445526244552Humanname
597761125CV3685626single nucleotide variantNM_001024598.4(HES3):c.31G>C (p.Val11Leu)not specified [RCV004925839]uncertain significance162443966244396Humanname
8629628CV84775single nucleotide variantNM_001024598.3(HES3):c.40G>A (p.Glu14Lys)Malignant melanoma [RCV000064857]not provided162444056244405Humanname
155959209CV2313885single nucleotide variantNM_001024598.4(HES3):c.197C>T (p.Pro66Leu)not specified [RCV004164198]uncertain significance162451436245143Humanname
329353179CV2468903single nucleotide variantNM_001024598.4(HES3):c.181A>G (p.Arg61Gly)not specified [RCV004280520]uncertain significance162451276245127Humanname
405803233CV3273840single nucleotide variantNM_001024598.4(HES3):c.238C>A (p.Leu80Ile)not specified [RCV004404336]uncertain significance162451846245184Humanname
405803234CV3273841single nucleotide variantNM_001024598.4(HES3):c.245G>A (p.Arg82His)not specified [RCV004404337]uncertain significance162451916245191Humanname
405803236CV3273842single nucleotide variantNM_001024598.4(HES3):c.271C>T (p.Arg91Cys)not specified [RCV004404338]uncertain significance162452176245217Humanname
597761120CV3685625single nucleotide variantNM_001024598.4(HES3):c.197C>A (p.Pro66Gln)not specified [RCV004925838]uncertain significance162451436245143Humanname
598275145CV3978654single nucleotide variantNM_001024598.4(HES3):c.190G>C (p.Glu64Gln)not specified [RCV005351776]uncertain significance162451366245136Humanname
156160280CV2236328single nucleotide variantNM_001024598.4(HES3):c.338C>A (p.Ala113Glu)not specified [RCV004108021]uncertain significance162452846245284Humanname
156233799CV2245292single nucleotide variantNM_001024598.4(HES3):c.371T>G (p.Val124Gly)not specified [RCV004107053]uncertain significance162453176245317Humanname
156248492CV2276989single nucleotide variantNM_001024598.4(HES3):c.415C>T (p.Pro139Ser)not specified [RCV004140317]uncertain significance162453616245361Humanname
155902648CV2386292single nucleotide variantNM_001024598.4(HES3):c.344C>T (p.Ala115Val)not specified [RCV004228638]uncertain significance162452906245290Humanname
329398022CV2464703single nucleotide variantNM_001024598.4(HES3):c.527G>A (p.Arg176Gln)not specified [RCV004284677]uncertain significance162454736245473Humanname
401870472CV2792385single nucleotide variantNM_001024598.4(HES3):c.308C>A (p.Thr103Asn)not specified [RCV004361549]uncertain significance162452546245254Humanname
405803238CV3273843single nucleotide variantNM_001024598.4(HES3):c.301G>C (p.Gly101Arg)not specified [RCV004404339]uncertain significance162452476245247Humanname
407521795CV3437171single nucleotide variantNM_001024598.4(HES3):c.449C>T (p.Ser150Leu)not specified [RCV004630489]uncertain significance162453956245395Humanname
407521798CV3437172single nucleotide variantNM_001024598.4(HES3):c.549T>A (p.Asp183Glu)not specified [RCV004630490]uncertain significance162454956245495Humanname
597761115CV3685624single nucleotide variantNM_001024598.4(HES3):c.512G>A (p.Gly171Asp)not specified [RCV004925837]uncertain significance162454586245458Humanname