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15 records found for search term Ppat
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15148116CV744156single nucleotide variantNM_002703.5(PPAT):c.128+10A>Tnot provided [RCV000900654]likely benign45643534056435340Humanname
598159794CV3901146single nucleotide variantNM_002703.5(PPAT):c.95T>C (p.Val32Ala)not specified [RCV005260827]uncertain significance45643538356435383Humanname
155971440CV2334217single nucleotide variantNM_002703.5(PPAT):c.188C>T (p.Ser63Leu)not specified [RCV004186202]uncertain significance45640765756407657Humanname
405793929CV3370075single nucleotide variantNM_002703.5(PPAT):c.233A>G (p.Asn78Ser)not specified [RCV004506890]uncertain significance45640666456406664Humanname
156083712CV2381912single nucleotide variantNM_002703.5(PPAT):c.879G>A (p.Met293Ile)not specified [RCV004225851]likely benign45640133756401337Humanname
329353192CV2468918single nucleotide variantNM_002703.5(PPAT):c.539C>T (p.Ala180Val)not specified [RCV004274190]uncertain significance45640316256403162Humanname
401745059CV2698456single nucleotide variantNM_002703.5(PPAT):c.497C>T (p.Thr166Ile)not specified [RCV004298967]uncertain significance45640330756403307Humanname
405793932CV3370076single nucleotide variantNM_002703.5(PPAT):c.806T>C (p.Ile269Thr)not specified [RCV004506891]uncertain significance45640141056401410Humanname
407529487CV3471328single nucleotide variantNM_002703.5(PPAT):c.973C>A (p.Pro325Thr)not specified [RCV004656068]uncertain significance45640082556400825Humanname
598159799CV3901147single nucleotide variantNM_002703.5(PPAT):c.742C>T (p.Arg248Cys)not specified [RCV005260828]uncertain significance45640147456401474Humanname
598159800CV3901148single nucleotide variantNM_002703.5(PPAT):c.628C>T (p.Arg210Cys)not specified [RCV005260829]uncertain significance45640307356403073Humanname
155991650CV2281124single nucleotide variantNM_002703.5(PPAT):c.1328C>T (p.Pro443Leu)not specified [RCV004147386]uncertain significance45639664856396648Humanname
405867029CV2842541single nucleotide variantNM_002703.5(PPAT):c.1051C>T (p.Arg351Trp)EBV-positive nodal T- and NK-cell lymphoma [RCV004557898]likely benign45639936456399364Humanname
405793927CV3370074single nucleotide variantNM_002703.5(PPAT):c.1327C>T (p.Pro443Ser)not specified [RCV004506889]uncertain significance45639664956396649Humanname
597757004CV3591052single nucleotide variantNM_002703.5(PPAT):c.1339C>G (p.His447Asp)not specified [RCV004848238]uncertain significance45639663756396637Humanname