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26 records found for search term Upk1b
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8577939CV112316single nucleotide variantNM_006952.3(UPK1B):c.648+2291G>TLung cancer [RCV000092839]uncertain significance3119196689119196689Humanname
405810312CV3345223single nucleotide variantNM_006952.4(UPK1B):c.26G>A (p.Arg9His)not specified [RCV004482183]uncertain significance3119186767119186767Humanname
156213178CV2257353single nucleotide variantNM_006952.4(UPK1B):c.92C>T (p.Ala31Val)not specified [RCV004125445]uncertain significance3119187797119187797Humanname
405810319CV3345227single nucleotide variantNM_006952.4(UPK1B):c.76G>A (p.Gly26Ser)not specified [RCV004482187]uncertain significance3119187781119187781Humanname
156044450CV2268526single nucleotide variantNM_006952.4(UPK1B):c.293T>C (p.Val98Ala)not specified [RCV004130210]uncertain significance3119190267119190267Humanname
156229036CV2273608single nucleotide variantNM_006952.4(UPK1B):c.130T>C (p.Tyr44His)not specified [RCV004134126]uncertain significance3119187835119187835Humanname
155929039CV2363417single nucleotide variantNM_006952.4(UPK1B):c.243G>C (p.Met81Ile)not specified [RCV004215999]uncertain significance3119187948119187948Humanname
155933005CV2399247single nucleotide variantNM_006952.4(UPK1B):c.239T>A (p.Ile80Asn)not specified [RCV004242546]uncertain significance3119187944119187944Humanname
405810310CV3345222single nucleotide variantNM_006952.4(UPK1B):c.269C>T (p.Ala90Val)not specified [RCV004482182]uncertain significance3119187974119187974Humanname
405810313CV3345224single nucleotide variantNM_006952.4(UPK1B):c.281T>C (p.Leu94Pro)not specified [RCV004482184]uncertain significance3119190255119190255Humanname
598191599CV3925773single nucleotide variantNM_006952.4(UPK1B):c.266T>G (p.Leu89Arg)not specified [RCV005288384]uncertain significance3119187971119187971Humanname
598191617CV3925777single nucleotide variantNM_006952.4(UPK1B):c.184G>A (p.Gly62Ser)not specified [RCV005288387]uncertain significance3119187889119187889Humanname
155924296CV2280518single nucleotide variantNM_006952.4(UPK1B):c.446C>T (p.Thr149Ile)not specified [RCV004142719]uncertain significance3119191082119191082Humanname
155904519CV2353894single nucleotide variantNM_006952.4(UPK1B):c.501C>G (p.Asp167Glu)not specified [RCV004201892]uncertain significance3119194251119194251Humanname
156237689CV2356202single nucleotide variantNM_006952.4(UPK1B):c.683G>A (p.Arg228Gln)not specified [RCV004206021]uncertain significance3119199091119199091Humanname
329358737CV2450681single nucleotide variantNM_006952.4(UPK1B):c.775G>A (p.Glu259Lys)not specified [RCV004267633]uncertain significance3119203959119203959Humanname
401764552CV2721372single nucleotide variantNM_006952.4(UPK1B):c.581A>G (p.Asn194Ser)not specified [RCV004322121]uncertain significance3119194331119194331Humanname
405810315CV3345225single nucleotide variantNM_006952.4(UPK1B):c.676A>G (p.Met226Val)not specified [RCV004482185]uncertain significance3119199084119199084Humanname
405810317CV3345226single nucleotide variantNM_006952.4(UPK1B):c.760T>C (p.Tyr254His)not specified [RCV004482186]uncertain significance3119203944119203944Humanname
405810321CV3345228single nucleotide variantNM_006952.4(UPK1B):c.773T>C (p.Ile258Thr)not specified [RCV004482188]uncertain significance3119203957119203957Humanname
597721604CV3629189single nucleotide variantNM_006952.4(UPK1B):c.329C>G (p.Ala110Gly)not specified [RCV004887928]uncertain significance3119190303119190303Humanname
597790958CV3629190single nucleotide variantNM_006952.4(UPK1B):c.749G>A (p.Gly250Asp)not specified [RCV004876493]uncertain significance3119203933119203933Humanname
597790961CV3629191single nucleotide variantNM_006952.4(UPK1B):c.562C>G (p.Arg188Gly)not specified [RCV004876494]uncertain significance3119194312119194312Humanname
598191605CV3925774single nucleotide variantNM_006952.4(UPK1B):c.616A>C (p.Lys206Gln)not specified [RCV005288385]uncertain significance3119194366119194366Humanname
598274771CV3925775single nucleotide variantNM_006952.4(UPK1B):c.353C>T (p.Pro118Leu)not specified [RCV005304110]uncertain significance3119190989119190989Humanname
598191611CV3925776single nucleotide variantNM_006952.4(UPK1B):c.665T>A (p.Ile222Asn)not specified [RCV005288386]uncertain significance3119199073119199073Humanname