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Variants search result for Homo sapiens
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20 records found for search term Rgs16
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
329375981CV2467399single nucleotide variantNM_002928.4(RGS16):c.19G>A (p.Ala7Thr)not specified [RCV004287017]uncertain significance1182604241182604241Humanname
598188926CV3902551single nucleotide variantNM_002928.4(RGS16):c.32C>T (p.Thr11Ile)not specified [RCV005266645]uncertain significance1182604228182604228Humanname
155910062CV2369659single nucleotide variantNM_002928.4(RGS16):c.133G>A (p.Gly45Ser)not specified [RCV004215063]uncertain significance1182603251182603251Humanname
329384389CV2435049single nucleotide variantNM_002928.4(RGS16):c.145A>G (p.Ser49Gly)not specified [RCV004252700]likely benign1182603239182603239Humanname
329378647CV2463683single nucleotide variantNM_002928.4(RGS16):c.124T>C (p.Phe42Leu)not specified [RCV004279258]uncertain significance1182603260182603260Humanname
407508107CV3472816single nucleotide variantNM_002928.4(RGS16):c.254C>G (p.Thr85Arg)not specified [RCV004671937]uncertain significance1182602099182602099Humanname
597788057CV3586332single nucleotide variantNM_002928.4(RGS16):c.152A>G (p.Glu51Gly)not specified [RCV004855397]uncertain significance1182603232182603232Humanname
597775757CV3586334single nucleotide variantNM_002928.4(RGS16):c.259T>G (p.Phe87Val)not specified [RCV004852334]uncertain significance1182602094182602094Humanname
598188919CV3902550single nucleotide variantNM_002928.4(RGS16):c.267G>C (p.Glu89Asp)not specified [RCV005266644]uncertain significance1182602086182602086Humanname
156270708CV2290162single nucleotide variantNM_002928.4(RGS16):c.532C>T (p.Arg178Trp)not specified [RCV004152825]uncertain significance1182600369182600369Humanname
156095493CV2377959single nucleotide variantNM_002928.4(RGS16):c.478C>T (p.Arg160Cys)not specified [RCV004230524]uncertain significance1182600423182600423Humanname
401726299CV2672431single nucleotide variantNM_002928.4(RGS16):c.398A>G (p.Asp133Gly)not specified [RCV004285685]uncertain significance1182600503182600503Humanname
401719070CV2679407single nucleotide variantNM_002928.4(RGS16):c.551C>T (p.Ala184Val)not specified [RCV004285935]uncertain significance1182600350182600350Humanname
401774312CV2727801single nucleotide variantNM_002928.4(RGS16):c.539T>C (p.Leu180Pro)not specified [RCV004323827]uncertain significance1182600362182600362Humanname
405715572CV3309200single nucleotide variantNM_002928.4(RGS16):c.343C>A (p.His115Asn)not specified [RCV004449139]uncertain significance1182602010182602010Humanname
405715578CV3309201single nucleotide variantNM_002928.4(RGS16):c.419C>T (p.Thr140Met)not specified [RCV004449140]uncertain significance1182600482182600482Humanname
405715582CV3309202single nucleotide variantNM_002928.4(RGS16):c.544G>A (p.Ala182Thr)not specified [RCV004449141]uncertain significance1182600357182600357Humanname
597788054CV3586331single nucleotide variantNM_002928.4(RGS16):c.509G>A (p.Arg170His)not specified [RCV004855396]uncertain significance1182600392182600392Humanname
597788061CV3586333single nucleotide variantNM_002928.4(RGS16):c.394A>G (p.Ile132Val)not specified [RCV004855398]uncertain significance1182600507182600507Humanname
598188912CV3902549single nucleotide variantNM_002928.4(RGS16):c.601C>T (p.His201Tyr)not specified [RCV005266643]uncertain significance1182600300182600300Humanname