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15 records found for search term Cdipt
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156401390CV2207134single nucleotide variantNM_006319.5(CDIPT):c.80A>G (p.Tyr27Cys)not specified [RCV004087875]uncertain significance162986268429862684Humanname
329381621CV2441463single nucleotide variantNM_006319.5(CDIPT):c.64G>T (p.Ala22Ser)not specified [RCV004257258]uncertain significance162986270029862700Humanname
156358420CV2251089single nucleotide variantNM_006319.5(CDIPT):c.142G>A (p.Ala48Thr)not specified [RCV004123634]uncertain significance162986262229862622Humanname
156210316CV2259797single nucleotide variantNM_006319.5(CDIPT):c.199C>G (p.Leu67Val)not specified [RCV004117070]uncertain significance162986123929861239Humanname
156007904CV2365210single nucleotide variantNM_006319.5(CDIPT):c.229A>G (p.Met77Val)not specified [RCV004205221]uncertain significance162986120929861209Humanname
401771079CV2700844single nucleotide variantNM_006319.5(CDIPT):c.212C>T (p.Thr71Met)not specified [RCV004307121]uncertain significance162986122629861226Humanname
156387815CV2221623single nucleotide variantNM_006319.5(CDIPT):c.560C>T (p.Ser187Leu)not specified [RCV004096875]uncertain significance162985927129859271Humanname
155994494CV2253697single nucleotide variantNM_006319.5(CDIPT):c.575T>C (p.Ile192Thr)not specified [RCV004125364]uncertain significance162985925629859256Humanname
155902093CV2274625single nucleotide variantNM_006319.5(CDIPT):c.436G>T (p.Ala146Ser)not specified [RCV004139013]uncertain significance162985950229859502Humanname
156197347CV2357629single nucleotide variantNM_006319.5(CDIPT):c.596G>A (p.Arg199His)not specified [RCV004202890]uncertain significance162985923529859235Humanname
155928410CV2363278single nucleotide variantNM_006319.5(CDIPT):c.517C>T (p.Arg173Trp)not specified [RCV004603374]uncertain significance162985931429859314Humanname
401766475CV2679706single nucleotide variantNM_006319.5(CDIPT):c.413G>A (p.Arg138Lys)not specified [RCV004282176]uncertain significance162986058229860582Humanname
405722237CV3292854single nucleotide variantNM_006319.5(CDIPT):c.617C>T (p.Ala206Val)not specified [RCV004428295]uncertain significance162985921429859214Humanname
597795953CV3642081single nucleotide variantNM_006319.5(CDIPT):c.418G>T (p.Ala140Ser)not specified [RCV004903852]uncertain significance162985952029859520Humanname
598178978CV3947556single nucleotide variantNM_006319.5(CDIPT):c.340G>A (p.Val114Ile)not specified [RCV005310435]uncertain significance162986065529860655Humanname