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15 records found for search term Rab27b
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8636532CV91757single nucleotide variantNM_004163.4(RAB27B):c.528C>T (p.Thr176=)Malignant melanoma [RCV000071855]not provided185488928454889284Humanname
597775040CV3589023single nucleotide variantNM_004163.4(RAB27B):c.151G>A (p.Val51Met)not specified [RCV004852140]uncertain significance185487773654877736Humanname
597775044CV3589024single nucleotide variantNM_004163.4(RAB27B):c.238C>T (p.Arg80Trp)not specified [RCV004852141]uncertain significance185487945354879453Humanname
597775047CV3589025single nucleotide variantNM_004163.4(RAB27B):c.208C>T (p.Leu70Phe)not specified [RCV004852142]uncertain significance185487942354879423Humanname
156233127CV2227735single nucleotide variantNM_004163.4(RAB27B):c.496A>G (p.Thr166Ala)not specified [RCV004094121]uncertain significance185488925254889252Humanname
156169376CV2266745single nucleotide variantNM_004163.4(RAB27B):c.446G>T (p.Arg149Leu)not specified [RCV004137574]uncertain significance185488809754888097Humanname
156009045CV2361949single nucleotide variantNM_004163.4(RAB27B):c.442G>A (p.Ala148Thr)not specified [RCV004207718]uncertain significance185488809354888093Humanname
156018218CV2370244single nucleotide variantNM_004163.4(RAB27B):c.459C>A (p.Asp153Glu)not specified [RCV004213164]likely benign185488811054888110Humanname
156161040CV2371351single nucleotide variantNM_004163.4(RAB27B):c.574A>G (p.Thr192Ala)not specified [RCV004223356]uncertain significance185488933054889330Humanname
401741044CV2680535single nucleotide variantNM_004163.4(RAB27B):c.466G>A (p.Gly156Ser)not specified [RCV004291169]uncertain significance185488811754888117Humanname
401761273CV2706285single nucleotide variantNM_004163.4(RAB27B):c.583C>T (p.Pro195Ser)not specified [RCV004314946]uncertain significance185488933954889339Humanname
401885750CV2774499single nucleotide variantNM_004163.4(RAB27B):c.347A>G (p.Gln116Arg)not specified [RCV004349988]uncertain significance185488799854887998Humanname
407483775CV3461663single nucleotide variantNM_004163.4(RAB27B):c.631C>G (p.Pro211Ala)not specified [RCV004665006]uncertain significance185488938754889387Humanname
597775036CV3589022single nucleotide variantNM_004163.4(RAB27B):c.436C>T (p.Arg146Trp)not specified [RCV004852139]uncertain significance185488808754888087Humanname
598164107CV3898558single nucleotide variantNM_004163.4(RAB27B):c.587A>T (p.Asp196Val)not specified [RCV005261658]uncertain significance185488934354889343Humanname