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Variants search result for Homo sapiens
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8 records found for search term Sap18
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156337903CV2343116single nucleotide variantNM_005870.5(SAP18):c.26A>G (p.Gln9Arg)not specified [RCV004192708]uncertain significance132114057821140578Humanname
401775107CV2696220single nucleotide variantNM_005870.5(SAP18):c.14G>A (p.Gly5Glu)not specified [RCV004310262]uncertain significance132114056621140566Humanname
405723240CV3320542single nucleotide variantNM_005870.5(SAP18):c.16G>A (p.Val6Ile)not specified [RCV004450103]uncertain significance132114056821140568Humanname
155975398CV2235867single nucleotide variantNM_005870.5(SAP18):c.33G>T (p.Glu11Asp)not specified [RCV004111978]uncertain significance132114058521140585Humanname
156089535CV2392085single nucleotide variantNM_005870.5(SAP18):c.34C>A (p.Arg12Ser)not specified [RCV004237980]uncertain significance132114058621140586Humanname
598223261CV3903761single nucleotide variantNM_005870.5(SAP18):c.34C>T (p.Arg12Cys)not specified [RCV005273023]uncertain significance132114058621140586Humanname
598223268CV3903762single nucleotide variantNM_005870.5(SAP18):c.47G>A (p.Arg16His)not specified [RCV005273024]uncertain significance132114059921140599Humanname
597789756CV3604982single nucleotide variantNM_005870.5(SAP18):c.112C>T (p.Pro38Ser)not specified [RCV004855835]uncertain significance132114066421140664Humanname