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11 records found for search term Avpi1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405679553CV3294308single nucleotide variantNM_021732.3(AVPI1):c.71A>G (p.Lys24Arg)not specified [RCV004421350]uncertain significance109767983597679835Humanname
597803741CV3633272single nucleotide variantNM_021732.3(AVPI1):c.80C>T (p.Ser27Leu)not specified [RCV004881894]uncertain significance109767982697679826Humanname
156054874CV2320496single nucleotide variantNM_021732.3(AVPI1):c.100G>A (p.Ala34Thr)not specified [RCV004172129]uncertain significance109767980697679806Humanname
155931925CV2371056single nucleotide variantNM_021732.3(AVPI1):c.154G>A (p.Glu52Lys)not specified [RCV004220813]uncertain significance109767975297679752Humanname
329375604CV2431580single nucleotide variantNM_021732.3(AVPI1):c.281G>A (p.Arg94His)not specified [RCV004254730]uncertain significance109767962597679625Humanname
597803737CV3633255single nucleotide variantNM_021732.3(AVPI1):c.259C>T (p.His87Tyr)not specified [RCV004881892]uncertain significance109767964797679647Humanname
598264415CV3932518single nucleotide variantNM_021732.3(AVPI1):c.197G>A (p.Arg66His)not specified [RCV005301541]uncertain significance109767970997679709Humanname
329392374CV2438905single nucleotide variantNM_021732.3(AVPI1):c.388C>T (p.Arg130Cys)not specified [RCV004264433]uncertain significance109767792597677925Humanname
401885955CV2771528single nucleotide variantNM_021732.3(AVPI1):c.388C>G (p.Arg130Gly)not specified [RCV004348558]uncertain significance109767792597677925Humanname
405679548CV3294307single nucleotide variantNM_021732.3(AVPI1):c.326G>A (p.Ser109Asn)not specified [RCV004421349]uncertain significance109767798797677987Humanname
597803739CV3633262single nucleotide variantNM_021732.3(AVPI1):c.440A>G (p.His147Arg)not specified [RCV004881893]uncertain significance109767787397677873Humanname