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31 records found for search term Rnps1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407572800CV3497150single nucleotide variantNM_080594.4(RNPS1):c.228-3C>Gnot provided [RCV004698970]uncertain significance1622632902263290Humanname
15134701CV755014single nucleotide variantNM_080594.4(RNPS1):c.105A>T (p.Ser35=)not provided [RCV000920731]likely benign1622642982264298Humanname
155989475CV2352215single nucleotide variantNM_080594.4(RNPS1):c.91C>T (p.Arg31Cys)not specified [RCV004200696]uncertain significance1622643122264312Humanname
329387114CV2436270single nucleotide variantNM_080594.4(RNPS1):c.73G>A (p.Ala25Thr)not specified [RCV004251680]uncertain significance1622643302264330Humanname
15170119CV703564single nucleotide variantNM_080594.4(RNPS1):c.711C>T (p.Ala237=)not provided [RCV000949590]benign1622556922255692Humanname
156255405CV2229291single nucleotide variantNM_080594.4(RNPS1):c.295T>C (p.Ser99Pro)not specified [RCV004101091]uncertain significance1622632202263220Humanname
329352054CV2455676single nucleotide variantNM_080594.4(RNPS1):c.266C>G (p.Thr89Ser)not specified [RCV004276913]uncertain significance1622632492263249Humanname
401891197CV2778564single nucleotide variantNM_080594.4(RNPS1):c.209G>A (p.Ser70Asn)not specified [RCV004344216]uncertain significance1622641942264194Humanname
405717226CV3309616single nucleotide variantNM_080594.4(RNPS1):c.202G>A (p.Ala68Thr)not specified [RCV004449364]uncertain significance1622642012264201Humanname
598206827CV3906015single nucleotide variantNM_080594.4(RNPS1):c.125G>A (p.Arg42His)not specified [RCV005269925]uncertain significance1622642782264278Humanname
155912517CV2245568single nucleotide variantNM_080594.4(RNPS1):c.842C>T (p.Ser281Phe)not specified [RCV004109648]uncertain significance1622540402254040Humanname
155977893CV2246939single nucleotide variantNM_080594.4(RNPS1):c.622G>A (p.Val208Ile)not specified [RCV004112734]uncertain significance1622623322262332Humanname
156109848CV2261532single nucleotide variantNM_080594.4(RNPS1):c.565A>G (p.Met189Val)not specified [RCV004123962]uncertain significance1622623892262389Humanname
156340645CV2268151single nucleotide variantNM_080594.4(RNPS1):c.834G>T (p.Arg278Ser)not specified [RCV004138470]uncertain significance1622540482254048Humanname
156000858CV2383283single nucleotide variantNM_080594.4(RNPS1):c.354C>G (p.Ser118Arg)not specified [RCV004222331]uncertain significance1622631612263161Humanname
329367162CV2427250single nucleotide variantNM_080594.4(RNPS1):c.893G>A (p.Arg298His)not specified [RCV004248117]uncertain significance1622539892253989Humanname
329353822CV2439739single nucleotide variantNM_080594.4(RNPS1):c.779C>T (p.Pro260Leu)not specified [RCV004255746]uncertain significance1622556242255624Humanname
401735981CV2672792single nucleotide variantNM_080594.4(RNPS1):c.874C>T (p.Arg292Cys)not specified [RCV004281573]uncertain significance1622540082254008Humanname
401775101CV2696218single nucleotide variantNM_080594.4(RNPS1):c.353G>C (p.Ser118Thr)not specified [RCV004310260]uncertain significance1622631622263162Humanname
401748374CV2698369single nucleotide variantNM_080594.4(RNPS1):c.666C>A (p.His222Gln)not specified [RCV004304909]uncertain significance1622622882262288Humanname
401735087CV2699159single nucleotide variantNM_080594.4(RNPS1):c.383G>C (p.Arg128Pro)not specified [RCV004303659]uncertain significance1622631322263132Humanname
405717234CV3309617single nucleotide variantNM_080594.4(RNPS1):c.376C>T (p.Pro126Ser)not specified [RCV004449365]uncertain significance1622631392263139Humanname
405717240CV3309618single nucleotide variantNM_080594.4(RNPS1):c.422C>G (p.Ser141Cys)not specified [RCV004449366]uncertain significance1622628402262840Humanname
405717249CV3309619single nucleotide variantNM_080594.4(RNPS1):c.665A>G (p.His222Arg)not specified [RCV004449367]uncertain significance1622622892262289Humanname
405717260CV3309620single nucleotide variantNM_080594.4(RNPS1):c.875G>A (p.Arg292His)not specified [RCV004449368]uncertain significance1622540072254007Humanname
405717270CV3309621single nucleotide variantNM_080594.4(RNPS1):c.878G>A (p.Arg293His)not specified [RCV004449369]uncertain significance1622540042254004Humanname
407487054CV3479823single nucleotide variantNM_080594.4(RNPS1):c.353G>A (p.Ser118Asn)not specified [RCV004665565]uncertain significance1622631622263162Humanname
407487060CV3479824single nucleotide variantNM_080594.4(RNPS1):c.385C>T (p.Arg129Cys)not specified [RCV004665566]uncertain significance1622631302263130Humanname
597688789CV3586772single nucleotide variantNM_080594.4(RNPS1):c.359C>T (p.Ser120Phe)not specified [RCV004858638]uncertain significance1622631562263156Humanname
597755677CV3586773single nucleotide variantNM_080594.4(RNPS1):c.647C>A (p.Ala216Asp)not specified [RCV004847671]uncertain significance1622623072262307Humanname
598206832CV3906016single nucleotide variantNM_080594.4(RNPS1):c.775C>T (p.Pro259Ser)not specified [RCV005269926]uncertain significance1622556282255628Humanname