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13 records found for search term Aadat
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156299497CV2326084single nucleotide variantNM_016228.4(AADAT):c.65T>A (p.Met22Lys)not specified [RCV004180371]uncertain significance4170089626170089626Humanname
401894189CV2770472single nucleotide variantNM_016228.4(AADAT):c.199A>T (p.Met67Leu)not specified [RCV004358109]uncertain significance4170088433170088433Humanname
155988951CV2234264single nucleotide variantNM_016228.4(AADAT):c.634C>T (p.Arg212Cys)not specified [RCV004106337]uncertain significance4170073156170073156Humanname
405703497CV3301158single nucleotide variantNM_016228.4(AADAT):c.381G>T (p.Met127Ile)not specified [RCV004425756]uncertain significance4170078572170078572Humanname
405704198CV3301247single nucleotide variantNM_016228.4(AADAT):c.964G>C (p.Val322Leu)not specified [RCV004425845]uncertain significance4170066477170066477Humanname
407532335CV3492994single nucleotide variantNM_016228.4(AADAT):c.443G>C (p.Ser148Thr)not specified [RCV004682979]uncertain significance4170078510170078510Humanname
597681686CV3621527single nucleotide variantNM_016228.4(AADAT):c.850G>C (p.Val284Leu)not specified [RCV004883656]uncertain significance4170068641170068641Humanname
598246876CV3911957single nucleotide variantNM_016228.4(AADAT):c.977A>G (p.Tyr326Cys)not specified [RCV005277192]uncertain significance4170066464170066464Humanname
8631088CV86244single nucleotide variantNM_016228.3(AADAT):c.515G>A (p.Arg172Lys)Malignant melanoma [RCV000066335]not provided4170073275170073275Humanname
329371923CV2454989single nucleotide variantNM_016228.4(AADAT):c.1065T>A (p.Phe355Leu)not specified [RCV004272254]uncertain significance4170064788170064788Humanname
407454844CV3489418single nucleotide variantNM_016228.4(AADAT):c.1246G>T (p.Val416Leu)not specified [RCV004685260]uncertain significance4170060960170060960Humanname
597788811CV3618208single nucleotide variantNM_016228.4(AADAT):c.1261A>G (p.Ile421Val)not specified [RCV004875947]uncertain significance4170060945170060945Humanname
598263031CV3919227single nucleotide variantNM_016228.4(AADAT):c.1165G>A (p.Val389Ile)not specified [RCV005280377]likely benign4170061963170061963Humanname