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38 records found for search term Snx17
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401910902CV2815626single nucleotide variantNM_014748.4(SNX17):c.432+8G>Anot provided [RCV003425548]likely benign22737397927373979Humanname
405259083CV3194505single nucleotide variantNM_014748.4(SNX17):c.318A>G (p.Gln106=)SNX17-related disorder [RCV003893902]likely benign22737330827373308Humanname , trait , alternate_id
405282418CV3212910single nucleotide variantNM_014748.4(SNX17):c.873C>T (p.Ser291=)SNX17-related disorder [RCV003957031]likely benign22737560427375604Humanname , trait , alternate_id
405732692CV3322583single nucleotide variantNM_014748.4(SNX17):c.53C>T (p.Ser18Phe)not specified [RCV004464545]uncertain significance22737079627370796Humanname
8630289CV85444single nucleotide variantNM_014748.3(SNX17):c.354C>T (p.Ser118=)Malignant melanoma [RCV000065527]not provided22737389327373893Humanname
401761566CV2699346single nucleotide variantNM_014748.4(SNX17):c.181C>G (p.Pro61Ala)not specified [RCV004305934]uncertain significance22737266527372665Humanname
405732675CV3322581single nucleotide variantNM_014748.4(SNX17):c.164T>C (p.Val55Ala)not specified [RCV004464543]uncertain significance22737264827372648Humanname
598171686CV3911680single nucleotide variantNM_014748.4(SNX17):c.273G>T (p.Leu91Phe)not specified [RCV005284915]uncertain significance22737326327373263Humanname
156282912CV2230851single nucleotide variantNM_014748.4(SNX17):c.949C>T (p.Arg317Cys)not specified [RCV004092332]uncertain significance22737568027375680Humanname
156367931CV2266902single nucleotide variantNM_014748.4(SNX17):c.529C>T (p.Arg177Trp)not specified [RCV004131565]uncertain significance22737435127374351Humanname
156123928CV2285718single nucleotide variantNM_014748.4(SNX17):c.644T>C (p.Met215Thr)not specified [RCV004141868]uncertain significance22737472127374721Humanname
156169403CV2296610single nucleotide variantNM_014748.4(SNX17):c.817C>T (p.Arg273Cys)not specified [RCV004154671]uncertain significance22737554827375548Humanname
156202006CV2300596single nucleotide variantNM_014748.4(SNX17):c.530G>A (p.Arg177Gln)not specified [RCV004155556]uncertain significance22737435227374352Humanname
156054726CV2388627single nucleotide variantNM_014748.4(SNX17):c.563C>G (p.Ser188Cys)not specified [RCV004239508]uncertain significance22737438527374385Humanname
329374256CV2463470single nucleotide variantNM_014748.4(SNX17):c.358G>A (p.Glu120Lys)not specified [RCV004277299]uncertain significance22737389727373897Humanname
401732298CV2678060single nucleotide variantNM_014748.4(SNX17):c.875C>T (p.Ala292Val)not specified [RCV004296581]uncertain significance22737560627375606Humanname
401761304CV2706294single nucleotide variantNM_014748.4(SNX17):c.794C>T (p.Thr265Met)not specified [RCV004314955]uncertain significance22737552527375525Humanname
405732683CV3322582single nucleotide variantNM_014748.4(SNX17):c.500A>G (p.Glu167Gly)not specified [RCV004464544]uncertain significance22737415227374152Humanname
405732706CV3322584single nucleotide variantNM_014748.4(SNX17):c.950G>A (p.Arg317His)not specified [RCV004464546]uncertain significance22737568127375681Humanname
597745313CV3607256single nucleotide variantNM_014748.4(SNX17):c.346G>C (p.Glu116Gln)not specified [RCV004865645]uncertain significance22737388527373885Humanname
597741042CV3607258single nucleotide variantNM_014748.4(SNX17):c.626C>T (p.Ala209Val)not specified [RCV004864780]uncertain significance22737470327374703Humanname
598171670CV3911677single nucleotide variantNM_014748.4(SNX17):c.818G>A (p.Arg273His)not specified [RCV005284912]uncertain significance22737554927375549Humanname
598171675CV3911678single nucleotide variantNM_014748.4(SNX17):c.505G>A (p.Glu169Lys)not specified [RCV005284913]uncertain significance22737415727374157Humanname
598171680CV3911679single nucleotide variantNM_014748.4(SNX17):c.734G>A (p.Arg245Gln)not specified [RCV005284914]uncertain significance22737511327375113Humanname
156274854CV2316409single nucleotide variantNM_014748.4(SNX17):c.1025G>A (p.Gly342Asp)not specified [RCV004169903]uncertain significance22737589227375892Humanname
401752100CV2714116single nucleotide variantNM_014748.4(SNX17):c.1237G>A (p.Val413Met)not specified [RCV004317372]uncertain significance22737636727376367Humanname
401890031CV2763599single nucleotide variantNM_014748.4(SNX17):c.1208C>T (p.Thr403Ile)not specified [RCV004343108]uncertain significance22737633827376338Humanname
405291007CV3203919single nucleotide variantNM_014748.4(SNX17):c.1223A>C (p.Asp408Ala)SNX17-related disorder [RCV003927361]likely benign22737635327376353Humanname , trait , alternate_id
405732616CV3322574single nucleotide variantNM_014748.4(SNX17):c.1168G>A (p.Gly390Ser)not specified [RCV004464536]uncertain significance22737616927376169Humanname
405732622CV3322575single nucleotide variantNM_014748.4(SNX17):c.1196G>A (p.Arg399Gln)not specified [RCV004464537]uncertain significance22737632627376326Humanname
405732631CV3322576single nucleotide variantNM_014748.4(SNX17):c.1255C>T (p.Leu419Phe)not specified [RCV004464538]uncertain significance22737638527376385Humanname
405732643CV3322577single nucleotide variantNM_014748.4(SNX17):c.1303A>C (p.Lys435Gln)not specified [RCV004464539]uncertain significance22737660927376609Humanname
405732650CV3322578single nucleotide variantNM_014748.4(SNX17):c.1396G>C (p.Gly466Arg)not specified [RCV004464540]uncertain significance22737670227376702Humanname
407525306CV3484798single nucleotide variantNM_014748.4(SNX17):c.1001C>T (p.Thr334Met)not specified [RCV004679128]uncertain significance22737586827375868Humanname
407525307CV3484799single nucleotide variantNM_014748.4(SNX17):c.1202G>C (p.Gly401Ala)not specified [RCV004679129]uncertain significance22737633227376332Humanname
407525308CV3484800single nucleotide variantNM_014748.4(SNX17):c.1073G>A (p.Arg358Gln)not specified [RCV004679130]uncertain significance22737594027375940Humanname
597745318CV3607257single nucleotide variantNM_014748.4(SNX17):c.1352C>T (p.Ala451Val)not specified [RCV004865646]uncertain significance22737665827376658Humanname
8630290CV85445single nucleotide variantNM_014748.3(SNX17):c.1373G>A (p.Gly458Asp)Malignant melanoma [RCV000065528]not provided22737667927376679Humanname