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Variants search result for Homo sapiens
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8 records found for search term Rab24
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155925139CV2211740single nucleotide variantNM_001031677.4(RAB24):c.517G>A (p.Val173Ile)not specified [RCV004084620]uncertain significance5177301955177301955Humanname
329398448CV2464591single nucleotide variantNM_001031677.4(RAB24):c.385C>G (p.Arg129Gly)not specified [RCV004278283]uncertain significance5177302445177302445Humanname
405679644CV3308591single nucleotide variantNM_001031677.4(RAB24):c.554A>G (p.Lys185Arg)not specified [RCV004443047]uncertain significance5177301801177301801Humanname
407483726CV3461655single nucleotide variantNM_001031677.4(RAB24):c.307G>C (p.Val103Leu)not specified [RCV004664999]uncertain significance5177302603177302603Humanname
597775000CV3589011single nucleotide variantNM_001031677.4(RAB24):c.419A>G (p.Gln140Arg)not specified [RCV004852129]uncertain significance5177302411177302411Humanname
597775004CV3589012single nucleotide variantNM_001031677.4(RAB24):c.486C>G (p.Asp162Glu)not specified [RCV004852130]uncertain significance5177301986177301986Humanname
597775007CV3589013single nucleotide variantNM_001031677.4(RAB24):c.326T>C (p.Leu109Pro)not specified [RCV004852131]uncertain significance5177302584177302584Humanname
598164042CV3898548single nucleotide variantNM_001031677.4(RAB24):c.388A>T (p.Arg130Trp)not specified [RCV005261648]uncertain significance5177302442177302442Humanname