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Variants search result for Homo sapiens
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10 records found for search term Rab33a
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401773712CV2727609single nucleotide variantNM_004794.3(RAB33A):c.8A>C (p.Gln3Pro)not specified [RCV004329794]uncertain significanceX130172070130172070Humanname
156033816CV2275164single nucleotide variantNM_004794.3(RAB33A):c.37C>T (p.Pro13Ser)not specified [RCV004136962]uncertain significanceX130172099130172099Humanname
407499829CV3461675single nucleotide variantNM_004794.3(RAB33A):c.148A>T (p.Thr50Ser)not specified [RCV004669404]uncertain significanceX130172210130172210Humanname
401769594CV2731447single nucleotide variantNM_004794.3(RAB33A):c.323G>A (p.Arg108His)not specified [RCV004330804]uncertain significanceX130184349130184349Humanname
401877083CV2769329single nucleotide variantNM_004794.3(RAB33A):c.686C>A (p.Ala229Asp)not specified [RCV004357325]uncertain significanceX130184712130184712Humanname
405680093CV3308627single nucleotide variantNM_004794.3(RAB33A):c.407A>G (p.Asn136Ser)not specified [RCV004443083]uncertain significanceX130184433130184433Humanname
405680087CV3308628single nucleotide variantNM_004794.3(RAB33A):c.658G>T (p.Val220Leu)not specified [RCV004443084]uncertain significanceX130184684130184684Humanname
407483847CV3461676single nucleotide variantNM_004794.3(RAB33A):c.302G>C (p.Ser101Thr)not specified [RCV004665017]uncertain significanceX130184328130184328Humanname
598164221CV3898574single nucleotide variantNM_004794.3(RAB33A):c.638C>T (p.Ala213Val)not specified [RCV005261674]uncertain significanceX130184664130184664Humanname
598164234CV3898576single nucleotide variantNM_004794.3(RAB33A):c.596C>T (p.Ala199Val)not specified [RCV005261676]uncertain significanceX130184622130184622Humanname