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Variants search result for Homo sapiens
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9 records found for search term Rab8a
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405680638CV3318784single nucleotide variantNM_005370.5(RAB8A):c.277G>A (p.Glu93Lys)not specified [RCV004443243]uncertain significance191612550016125500Humanname
407484182CV3461748single nucleotide variantNM_005370.5(RAB8A):c.224C>T (p.Thr75Met)not specified [RCV004665069]uncertain significance191612178816121788Humanname
156217776CV2253891single nucleotide variantNM_005370.5(RAB8A):c.401A>C (p.Glu134Ala)not specified [RCV004127572]uncertain significance191612751316127513Humanname
156017296CV2295563single nucleotide variantNM_005370.5(RAB8A):c.530T>C (p.Leu177Ser)not specified [RCV004160656]uncertain significance191612960316129603Humanname
329395943CV2463089single nucleotide variantNM_005370.5(RAB8A):c.514A>C (p.Lys172Gln)not specified [RCV004272897]uncertain significance191612958716129587Humanname
405680642CV3318785single nucleotide variantNM_005370.5(RAB8A):c.444G>A (p.Met148Ile)not specified [RCV004443244]uncertain significance191612805516128055Humanname
405680656CV3318787single nucleotide variantNM_005370.5(RAB8A):c.488T>C (p.Phe163Ser)not specified [RCV004443246]uncertain significance191612956116129561Humanname
597775436CV3589168single nucleotide variantNM_005370.5(RAB8A):c.403C>T (p.Arg135Trp)not specified [RCV004852249]uncertain significance191612751516127515Humanname
598164725CV3908603single nucleotide variantNM_005370.5(RAB8A):c.352A>G (p.Ile118Val)not specified [RCV005261760]uncertain significance191612746416127464Humanname