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18 records found for search term Ddi2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401907431CV2805770single nucleotide variantNM_032341.5(DDI2):c.90C>T (p.Phe30=)not provided [RCV003422635]uncertain significance11561776015617760Humanname
597801278CV3661900single nucleotide variantNM_032341.5(DDI2):c.5T>A (p.Leu2Gln)not specified [RCV004906122]uncertain significance11561767515617675Humanname
155930198CV2224683single nucleotide variantNM_032341.5(DDI2):c.281T>C (p.Ile94Thr)not specified [RCV004092522]uncertain significance11563033715630337Humanname
401907432CV2805771single nucleotide variantNM_032341.5(DDI2):c.1116T>C (p.Asp372=)not provided [RCV003422636]likely benign11565182815651828Humanname
155989202CV2259669single nucleotide variantNM_032341.5(DDI2):c.350A>T (p.Gln117Leu)not specified [RCV004116701]uncertain significance11563040615630406Humanname
156104673CV2260594single nucleotide variantNM_032341.5(DDI2):c.356A>G (p.His119Arg)not specified [RCV004123364]uncertain significance11563041215630412Humanname
156079635CV2292617single nucleotide variantNM_032341.5(DDI2):c.449C>G (p.Ser150Cys)not specified [RCV004154307]uncertain significance11563050515630505Humanname
401747885CV2699944single nucleotide variantNM_032341.5(DDI2):c.958A>G (p.Met320Val)not specified [RCV004310387]uncertain significance11564978815649788Humanname
597801272CV3661896single nucleotide variantNM_032341.5(DDI2):c.329G>A (p.Arg110His)not specified [RCV004906119]uncertain significance11563038515630385Humanname
597801274CV3661897single nucleotide variantNM_032341.5(DDI2):c.322C>T (p.Arg108Trp)not specified [RCV004906120]uncertain significance11563037815630378Humanname
597801276CV3661898single nucleotide variantNM_032341.5(DDI2):c.932C>G (p.Ser311Cys)not specified [RCV004906121]uncertain significance11564976215649762Humanname
597801280CV3661901single nucleotide variantNM_032341.5(DDI2):c.650A>C (p.Glu217Ala)not specified [RCV004906123]uncertain significance11563832415638324Humanname
598262955CV3959925single nucleotide variantNM_032341.5(DDI2):c.323G>A (p.Arg108Gln)not specified [RCV005325531]uncertain significance11563037915630379Humanname
598262961CV3959927single nucleotide variantNM_032341.5(DDI2):c.551G>A (p.Arg184Gln)not specified [RCV005325533]uncertain significance11563348415633484Humanname
598262964CV3959928single nucleotide variantNM_032341.5(DDI2):c.493A>T (p.Ser165Cys)not specified [RCV005325534]uncertain significance11563054915630549Humanname
598262967CV3959929single nucleotide variantNM_032341.5(DDI2):c.985C>T (p.Arg329Trp)not specified [RCV005325535]uncertain significance11564981515649815Humanname
405702932CV3243488single nucleotide variantNM_032341.5(DDI2):c.1190A>G (p.Gln397Arg)not specified [RCV004375544]uncertain significance11565662315656623Humanname
597783347CV3661899single nucleotide variantNM_032341.5(DDI2):c.1109G>A (p.Arg370Lys)not specified [RCV004900167]uncertain significance11565182115651821Humanname