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8 records found for search term Ppp1r1c
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405652638CV3376833single nucleotide variantNM_001080545.3(PPP1R1C):c.37G>A (p.Val13Met)not specified [RCV004509868]uncertain significance2181986147181986147Humanname
156356978CV2253782single nucleotide variantNM_001080545.3(PPP1R1C):c.101C>A (p.Thr34Lys)not specified [RCV004127486]uncertain significance2181987858181987858Humanname
156047066CV2382402single nucleotide variantNM_001080545.3(PPP1R1C):c.268G>A (p.Glu90Lys)not specified [RCV004230740]uncertain significance2182117233182117233Humanname
401876707CV2783037single nucleotide variantNM_001080545.3(PPP1R1C):c.131A>G (p.His44Arg)not specified [RCV004361818]uncertain significance2181987888181987888Humanname
405652634CV3376831single nucleotide variantNM_001080545.3(PPP1R1C):c.125A>G (p.Asn42Ser)not specified [RCV004509866]uncertain significance2181987882181987882Humanname
405652636CV3376832single nucleotide variantNM_001080545.3(PPP1R1C):c.235A>G (p.Ile79Val)not specified [RCV004509867]uncertain significance2182063785182063785Humanname
598169565CV3897620single nucleotide variantNM_001080545.3(PPP1R1C):c.323A>G (p.Asp108Gly)not specified [RCV005262829]uncertain significance2182117288182117288Humanname
598169569CV3897621single nucleotide variantNM_001080545.3(PPP1R1C):c.316C>G (p.Gln106Glu)not specified [RCV005262830]uncertain significance2182117281182117281Humanname