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39 records found for search term Scamp3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597689510CV3601596single nucleotide variantNM_005698.4(SCAMP3):c.14G>C (p.Arg5Thr)not specified [RCV004858711]uncertain significance1155262138155262138Humanname
156160563CV2236358single nucleotide variantNM_005698.4(SCAMP3):c.70C>T (p.Pro24Ser)not specified [RCV004108044]uncertain significance1155261731155261731Humanname
597689499CV3601595single nucleotide variantNM_005698.4(SCAMP3):c.34G>C (p.Ala12Pro)not specified [RCV004858710]uncertain significance1155262118155262118Humanname
156121381CV2240820single nucleotide variantNM_005698.4(SCAMP3):c.239C>T (p.Pro80Leu)not specified [RCV004102115]uncertain significance1155260565155260565Humanname
156174051CV2284204single nucleotide variantNM_005698.4(SCAMP3):c.209A>C (p.Gln70Pro)not specified [RCV004146575]uncertain significance1155260595155260595Humanname
401748503CV2704317single nucleotide variantNM_005698.4(SCAMP3):c.277G>C (p.Ala93Pro)not specified [RCV004311300]uncertain significance1155260441155260441Humanname
407461106CV3483838single nucleotide variantNM_005698.4(SCAMP3):c.202T>A (p.Ser68Thr)not specified [RCV004658626]uncertain significance1155260602155260602Humanname
597689488CV3601594single nucleotide variantNM_005698.4(SCAMP3):c.113T>C (p.Leu38Pro)not specified [RCV004858709]uncertain significance1155261688155261688Humanname
597689522CV3601597single nucleotide variantNM_005698.4(SCAMP3):c.215C>T (p.Ser72Leu)not specified [RCV004858712]uncertain significance1155260589155260589Humanname
598195997CV3900239single nucleotide variantNM_005698.4(SCAMP3):c.284C>T (p.Ala95Val)not specified [RCV005267860]uncertain significance1155260434155260434Humanname
598196002CV3900240single nucleotide variantNM_005698.4(SCAMP3):c.287C>T (p.Thr96Ile)not specified [RCV005267861]uncertain significance1155260431155260431Humanname
598196007CV3900241single nucleotide variantNM_005698.4(SCAMP3):c.277G>A (p.Ala93Thr)not specified [RCV005267862]uncertain significance1155260441155260441Humanname
156399434CV2205116single nucleotide variantNM_005698.4(SCAMP3):c.839T>C (p.Leu280Pro)not specified [RCV004077715]uncertain significance1155256732155256732Humanname
156074534CV2247852single nucleotide variantNM_005698.4(SCAMP3):c.904T>G (p.Ser302Ala)not specified [RCV004121312]uncertain significance1155256413155256413Humanname
156192325CV2255357single nucleotide variantNM_005698.4(SCAMP3):c.352C>G (p.Arg118Gly)not specified [RCV004117727]uncertain significance1155260366155260366Humanname
156044407CV2268523single nucleotide variantNM_005698.4(SCAMP3):c.922G>A (p.Gly308Ser)not specified [RCV004130207]uncertain significance1155256395155256395Humanname
155993479CV2281326single nucleotide variantNM_005698.4(SCAMP3):c.847G>A (p.Ala283Thr)not specified [RCV004147555]uncertain significance1155256724155256724Humanname
155908355CV2302409single nucleotide variantNM_005698.4(SCAMP3):c.989C>T (p.Thr330Ile)not specified [RCV004161152]uncertain significance1155256328155256328Humanname
156162971CV2311867single nucleotide variantNM_005698.4(SCAMP3):c.548T>A (p.Leu183His)not specified [RCV004170706]uncertain significance1155257627155257627Humanname
156275056CV2318203single nucleotide variantNM_005698.4(SCAMP3):c.415C>T (p.Pro139Ser)not specified [RCV004179388]uncertain significance1155258928155258928Humanname
156148172CV2321680single nucleotide variantNM_005698.4(SCAMP3):c.895C>T (p.Arg299Trp)not specified [RCV004179685]uncertain significance1155256676155256676Humanname
156107992CV2355368single nucleotide variantNM_005698.4(SCAMP3):c.848C>T (p.Ala283Val)not specified [RCV004205230]uncertain significance1155256723155256723Humanname
329396909CV2468318single nucleotide variantNM_005698.4(SCAMP3):c.917G>A (p.Arg306His)not specified [RCV004275868]uncertain significance1155256400155256400Humanname
401717667CV2710441single nucleotide variantNM_005698.4(SCAMP3):c.454A>T (p.Ile152Phe)not specified [RCV004317595]uncertain significance1155258889155258889Humanname
405742495CV3317076single nucleotide variantNM_005698.4(SCAMP3):c.322C>T (p.Arg108Trp)not specified [RCV004452597]uncertain significance1155260396155260396Humanname
405742502CV3317077single nucleotide variantNM_005698.4(SCAMP3):c.500T>C (p.Met167Thr)not specified [RCV004452598]uncertain significance1155258843155258843Humanname
405742509CV3317078single nucleotide variantNM_005698.4(SCAMP3):c.656G>A (p.Arg219His)not specified [RCV004452599]uncertain significance1155257519155257519Humanname
405742516CV3317079single nucleotide variantNM_005698.4(SCAMP3):c.736C>T (p.Leu246Phe)not specified [RCV004452600]uncertain significance1155257328155257328Humanname
405742520CV3317080single nucleotide variantNM_005698.4(SCAMP3):c.797T>C (p.Leu266Pro)not specified [RCV004452601]uncertain significance1155256774155256774Humanname
405742528CV3317081single nucleotide variantNM_005698.4(SCAMP3):c.806C>T (p.Pro269Leu)not specified [RCV004452602]likely benign1155256765155256765Humanname
405742535CV3317082single nucleotide variantNM_005698.4(SCAMP3):c.812G>A (p.Gly271Asp)not specified [RCV004452603]uncertain significance1155256759155256759Humanname
405742540CV3317083single nucleotide variantNM_005698.4(SCAMP3):c.847G>T (p.Ala283Ser)not specified [RCV004452604]uncertain significance1155256724155256724Humanname
405742548CV3317084single nucleotide variantNM_005698.4(SCAMP3):c.896G>A (p.Arg299Gln)not specified [RCV004452605]uncertain significance1155256675155256675Humanname
405742555CV3317085single nucleotide variantNM_005698.4(SCAMP3):c.956C>T (p.Ala319Val)not specified [RCV004452606]uncertain significance1155256361155256361Humanname
597689468CV3601592single nucleotide variantNM_005698.4(SCAMP3):c.898A>G (p.Ile300Val)not specified [RCV004858707]uncertain significance1155256419155256419Humanname
598195992CV3900238single nucleotide variantNM_005698.4(SCAMP3):c.392G>C (p.Arg131Pro)not specified [RCV005267859]uncertain significance1155258951155258951Humanname
598196012CV3900242single nucleotide variantNM_005698.4(SCAMP3):c.662T>C (p.Met221Thr)not specified [RCV005267863]uncertain significance1155257513155257513Humanname
329373733CV2447366single nucleotide variantNM_005698.4(SCAMP3):c.1034G>A (p.Arg345Gln)not specified [RCV004262644]uncertain significance1155256283155256283Humanname
597689477CV3601593single nucleotide variantNM_005698.4(SCAMP3):c.1001A>G (p.Asn334Ser)not specified [RCV004858708]uncertain significance1155256316155256316Humanname