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56 records found for search term Snx29
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156050253CV2391154single nucleotide variantNM_032167.5(SNX29):c.80G>A (p.Arg27His)not specified [RCV004237178]uncertain significance161200300112003001Humanname
401911500CV2807648single nucleotide variantNM_032167.5(SNX29):c.585C>G (p.Leu195=)not provided [RCV003426594]likely benign161204845712048457Humanname
401934445CV2807649single nucleotide variantNM_032167.5(SNX29):c.711C>T (p.Thr237=)not provided [RCV003411276]likely benign161204858312048583Humanname
8635664CV90886single nucleotide variantNM_032167.4(SNX29):c.687C>T (p.Ile229=)Malignant melanoma [RCV000070984]not provided161204855912048559Humanname
156089662CV2202078single nucleotide variantNM_032167.5(SNX29):c.154G>A (p.Val52Ile)not specified [RCV004075992]uncertain significance161202735112027351Humanname
329381977CV2467445single nucleotide variantNM_032167.5(SNX29):c.268G>A (p.Val90Met)not specified [RCV004287055]uncertain significance161204291712042917Humanname
401911502CV2807652single nucleotide variantNM_032167.5(SNX29):c.2349C>T (p.Asn783=)not provided [RCV003426596]likely benign161256853612568536Humanname
405733300CV3322661single nucleotide variantNM_032167.5(SNX29):c.253G>A (p.Val85Met)not specified [RCV004464623]uncertain significance161204290212042902Humanname
598172148CV3911748single nucleotide variantNM_032167.5(SNX29):c.250C>T (p.Pro84Ser)not specified [RCV005284977]uncertain significance161204289912042899Humanname
156321179CV2197520single nucleotide variantNM_032167.5(SNX29):c.841G>A (p.Val281Met)not specified [RCV004081244]uncertain significance161205193912051939Humanname
156330440CV2227014single nucleotide variantNM_032167.5(SNX29):c.916G>A (p.Ala306Thr)not specified [RCV004097400]uncertain significance161205201412052014Humanname
156128907CV2283943single nucleotide variantNM_032167.5(SNX29):c.392A>G (p.Tyr131Cys)not specified [RCV004144255]uncertain significance161204304112043041Humanname
156173214CV2284054single nucleotide variantNM_032167.5(SNX29):c.746C>T (p.Ala249Val)not specified [RCV004144660]uncertain significance161204861812048618Humanname
156010657CV2291053single nucleotide variantNM_032167.5(SNX29):c.359G>A (p.Arg120His)not specified [RCV004151586]uncertain significance161204300812043008Humanname
155964095CV2308350single nucleotide variantNM_032167.5(SNX29):c.625G>C (p.Glu209Gln)not specified [RCV004164831]uncertain significance161204849712048497Humanname
156352895CV2324066single nucleotide variantNM_032167.5(SNX29):c.916G>T (p.Ala306Ser)not specified [RCV004178361]uncertain significance161205201412052014Humanname
156190708CV2339629single nucleotide variantNM_032167.5(SNX29):c.506A>G (p.Asn169Ser)not specified [RCV004196338]uncertain significance161204837812048378Humanname
155922615CV2340646single nucleotide variantNM_032167.5(SNX29):c.475A>G (p.Ser159Gly)not provided [RCV004695609]|not specified [RCV004190319]uncertain significance161204643012046430Humanname
156004407CV2357564single nucleotide variantNM_032167.5(SNX29):c.770G>T (p.Arg257Leu)not specified [RCV004202830]uncertain significance161205186812051868Humanname
156344660CV2364315single nucleotide variantNM_032167.5(SNX29):c.301C>T (p.Arg101Cys)not specified [RCV004223536]uncertain significance161204295012042950Humanname
156051174CV2367703single nucleotide variantNM_032167.5(SNX29):c.995A>C (p.Asn332Thr)not specified [RCV004211617]uncertain significance161205209312052093Humanname
156209159CV2370073single nucleotide variantNM_032167.5(SNX29):c.316C>T (p.Arg106Cys)not specified [RCV004210968]uncertain significance161204296512042965Humanname
155937752CV2373808single nucleotide variantNM_032167.5(SNX29):c.373G>A (p.Glu125Lys)not specified [RCV004224747]uncertain significance161204302212043022Humanname
156144932CV2383964single nucleotide variantNM_032167.5(SNX29):c.889G>A (p.Asp297Asn)not specified [RCV004224943]uncertain significance161205198712051987Humanname
329369079CV2424689single nucleotide variantNM_032167.5(SNX29):c.649C>G (p.Leu217Val)not specified [RCV004248586]uncertain significance161204852112048521Humanname
329376286CV2438076single nucleotide variantNM_032167.5(SNX29):c.679G>A (p.Val227Ile)not specified [RCV004256864]uncertain significance161204855112048551Humanname
329371360CV2458093single nucleotide variantNM_032167.5(SNX29):c.958A>G (p.Ser320Gly)not specified [RCV004271918]uncertain significance161205205612052056Humanname
401754109CV2685166single nucleotide variantNM_032167.5(SNX29):c.415C>T (p.Arg139Cys)not specified [RCV004289729]uncertain significance161204306412043064Humanname
401727027CV2692126single nucleotide variantNM_032167.5(SNX29):c.431C>T (p.Thr144Ile)not specified [RCV004301831]uncertain significance161204638612046386Humanname
401911501CV2807650single nucleotide variantNM_032167.5(SNX29):c.853A>T (p.Thr285Ser)not provided [RCV003426595]likely benign161205195112051951Humanname
405733308CV3322662single nucleotide variantNM_032167.5(SNX29):c.367C>G (p.Leu123Val)not specified [RCV004464624]uncertain significance161204301612043016Humanname
405733316CV3322663single nucleotide variantNM_032167.5(SNX29):c.400A>G (p.Met134Val)not specified [RCV004464625]uncertain significance161204304912043049Humanname
405733323CV3322664single nucleotide variantNM_032167.5(SNX29):c.412G>A (p.Asp138Asn)not specified [RCV004464626]uncertain significance161204306112043061Humanname
405733329CV3322665single nucleotide variantNM_032167.5(SNX29):c.892C>T (p.Arg298Cys)not specified [RCV004464627]uncertain significance161205199012051990Humanname
405733343CV3322667single nucleotide variantNM_032167.5(SNX29):c.947A>G (p.Asn316Ser)not specified [RCV004464629]uncertain significance161205204512052045Humanname
405733352CV3322668single nucleotide variantNM_032167.5(SNX29):c.997G>A (p.Gly333Arg)not specified [RCV004464630]uncertain significance161205209512052095Humanname
407525319CV3484834single nucleotide variantNM_032167.5(SNX29):c.803C>T (p.Ser268Leu)not specified [RCV004679141]uncertain significance161205190112051901Humanname
597756013CV3607326single nucleotide variantNM_032167.5(SNX29):c.507C>G (p.Asn169Lys)not specified [RCV004868173]uncertain significance161204837912048379Humanname
597741144CV3607328single nucleotide variantNM_032167.5(SNX29):c.329C>T (p.Ser110Leu)not specified [RCV004864802]uncertain significance161204297812042978Humanname
597741149CV3607329single nucleotide variantNM_032167.5(SNX29):c.770G>A (p.Arg257Gln)not specified [RCV004864803]uncertain significance161205186812051868Humanname
598172112CV3911740single nucleotide variantNM_032167.5(SNX29):c.844T>C (p.Phe282Leu)not specified [RCV005284970]uncertain significance161205194212051942Humanname
598172116CV3911741single nucleotide variantNM_032167.5(SNX29):c.967T>C (p.Ser323Pro)not specified [RCV005284971]uncertain significance161205206512052065Humanname
598238493CV3911742single nucleotide variantNM_032167.5(SNX29):c.973A>C (p.Lys325Gln)not specified [RCV005275842]uncertain significance161205207112052071Humanname
598172121CV3911743single nucleotide variantNM_032167.5(SNX29):c.389G>A (p.Arg130His)not specified [RCV005284972]uncertain significance161204303812043038Humanname
598172126CV3911744single nucleotide variantNM_032167.5(SNX29):c.397C>T (p.His133Tyr)not specified [RCV005284973]uncertain significance161204304612043046Humanname
598172138CV3911746single nucleotide variantNM_032167.5(SNX29):c.839A>T (p.Asp280Val)not specified [RCV005284975]uncertain significance161205193712051937Humanname
598172143CV3911747single nucleotide variantNM_032167.5(SNX29):c.404T>C (p.Leu135Pro)not specified [RCV005284976]uncertain significance161204305312043053Humanname
8635665CV90887single nucleotide variantNM_032167.4(SNX29):c.688C>T (p.Leu230Phe)Malignant melanoma [RCV000070985]not provided161204856012048560Humanname
156333199CV2214560single nucleotide variantNM_032167.5(SNX29):c.1117C>T (p.Pro373Ser)not specified [RCV004088608]uncertain significance161205221512052215Humanname
156069803CV2292831single nucleotide variantNM_032167.5(SNX29):c.1060G>A (p.Glu354Lys)not specified [RCV004148348]uncertain significance161205215812052158Humanname
156387617CV2372802single nucleotide variantNM_032167.5(SNX29):c.1115C>T (p.Ser372Leu)not specified [RCV004221987]uncertain significance161205221312052213Humanname
401916567CV2807651single nucleotide variantNM_032167.5(SNX29):c.1511C>T (p.Ala504Val)not provided [RCV003429123]likely benign161212967412129674Humanname
405733292CV3322660single nucleotide variantNM_032167.5(SNX29):c.1064A>G (p.Asp355Gly)not specified [RCV004464622]uncertain significance161205216212052162Humanname
407525318CV3484832single nucleotide variantNM_032167.5(SNX29):c.1097A>G (p.His366Arg)not specified [RCV004679140]uncertain significance161205219512052195Humanname
598172132CV3911745single nucleotide variantNM_032167.5(SNX29):c.1103G>T (p.Gly368Val)not specified [RCV005284974]uncertain significance161205220112052201Humanname
41405569CV981934deletionNM_032167.5(SNX29):c.1363_1364del (p.Leu455fs)not provided [RCV001813068]uncertain significance161207887612078877Humanname