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9 records found for search term Vamp8
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
150334248CV1171000single nucleotide variantNM_003761.5(VAMP8):c.*143T>Cnot provided [RCV001539917]benign28558185985581859Humanname
155929747CV2360959single nucleotide variantNM_003761.5(VAMP8):c.29A>G (p.Asn10Ser)not specified [RCV004216159]uncertain significance28557903485579034Humanname
405806127CV3348712single nucleotide variantNM_003761.5(VAMP8):c.35G>C (p.Arg12Pro)not specified [RCV004480044]uncertain significance28557904085579040Humanname
155992457CV2379314single nucleotide variantNM_003761.5(VAMP8):c.271A>G (p.Ile91Val)not specified [RCV004223779]uncertain significance28558168485581684Humanname
156092904CV2389630single nucleotide variantNM_003761.5(VAMP8):c.133C>T (p.Arg45Cys)not specified [RCV004243688]uncertain significance28557913885579138Humanname
401863447CV2765804single nucleotide variantNM_003761.5(VAMP8):c.119A>T (p.Asn40Ile)not specified [RCV004335799]uncertain significance28557912485579124Humanname
405806124CV3348711single nucleotide variantNM_003761.5(VAMP8):c.116A>G (p.Glu39Gly)not specified [RCV004480043]uncertain significance28557912185579121Humanname
407529344CV3493292single nucleotide variantNM_003761.5(VAMP8):c.225G>C (p.Lys75Asn)not specified [RCV004680849]uncertain significance28558163885581638Humanname
598205297CV3929348single nucleotide variantNM_003761.5(VAMP8):c.109C>T (p.Arg37Trp)not specified [RCV005290827]uncertain significance28557911485579114Humanname