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11 records found for search term Capzb
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401935427CV2812417single nucleotide variantNM_004930.5(CAPZB):c.93+4C>Tnot provided [RCV003412855]likely benign11941965719419657Humanname
401884753CV2766225single nucleotide variantNM_004930.5(CAPZB):c.731+1496C>Gnot specified [RCV004340664]uncertain significance11934286219342862Humanname
405713083CV3299104single nucleotide variantNM_004930.5(CAPZB):c.731+1520A>Gnot specified [RCV004427103]uncertain significance11934283819342838Humanname
405713091CV3299105single nucleotide variantNM_004930.5(CAPZB):c.731+1568G>Anot specified [RCV004427104]uncertain significance11934279019342790Humanname
597775607CV3644014single nucleotide variantNM_004930.5(CAPZB):c.731+1505C>Tnot specified [RCV004898281]likely benign11934285319342853Humanname
401935426CV2812416single nucleotide variantNM_004930.5(CAPZB):c.492C>T (p.Thr164=)not provided [RCV003412854]likely benign11935673119356731Humanname
156395220CV2325281single nucleotide variantNM_004930.5(CAPZB):c.320A>G (p.Tyr107Cys)not specified [RCV004177676]uncertain significance11937854919378549Humanname
401772401CV2712709single nucleotide variantNM_004930.5(CAPZB):c.460G>A (p.Val154Ile)not specified [RCV004308017]uncertain significance11935743319357433Humanname
405713077CV3299103single nucleotide variantNM_004930.5(CAPZB):c.491C>T (p.Thr164Ile)not specified [RCV004427102]uncertain significance11935673219356732Humanname
597775602CV3644013single nucleotide variantNM_004930.5(CAPZB):c.439T>A (p.Cys147Ser)not specified [RCV004898280]uncertain significance11935745419357454Humanname
598213063CV3939356single nucleotide variantNM_004930.5(CAPZB):c.644G>A (p.Arg215His)not specified [RCV005316261]uncertain significance11934519719345197Humanname