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10 records found for search term Arl15
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401923118CV2796630single nucleotide variantNM_019087.3(ARL15):c.253+3A>TARL15-related disorder [RCV003404249]uncertain significance55415457754154577Humanname , trait , alternate_id
405287926CV3218035single nucleotide variantNM_019087.3(ARL15):c.15A>G (p.Arg5=)ARL15-related disorder [RCV003982159]benign55431046554310465Human4name , trait , alternate_id
401771269CV2722773single nucleotide variantNM_019087.3(ARL15):c.89G>A (p.Arg30Gln)not specified [RCV004325201]uncertain significance55417188854171888Humanname
405662854CV3290115single nucleotide variantNM_019087.3(ARL15):c.95A>T (p.Glu32Val)not specified [RCV004417888]uncertain significance55417188254171882Humanname
401758878CV2705216single nucleotide variantNM_019087.3(ARL15):c.124G>A (p.Gly42Ser)not specified [RCV004311920]uncertain significance55417185354171853Humanname
329390581CV2437096single nucleotide variantNM_019087.3(ARL15):c.484G>C (p.Glu162Gln)not specified [RCV004262903]uncertain significance55388669253886692Humanname
405662841CV3290112single nucleotide variantNM_019087.3(ARL15):c.347T>C (p.Leu116Ser)not specified [RCV004417885]uncertain significance55411331754113317Humanname
405662844CV3290113single nucleotide variantNM_019087.3(ARL15):c.425A>G (p.Asn142Ser)not specified [RCV004417886]uncertain significance55411323954113239Humanname
405662849CV3290114single nucleotide variantNM_019087.3(ARL15):c.499G>A (p.Gly167Arg)not specified [RCV004417887]uncertain significance55388667753886677Humanname
598183261CV3901732single nucleotide variantNM_019087.3(ARL15):c.349G>A (p.Glu117Lys)not specified [RCV005265574]uncertain significance55411331554113315Humanname