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Variants search result for Homo sapiens
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110 records found for search term Cdh26
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8586581CV121185single nucleotide variantNM_021810.4(CDH26):c.294+514G>ALung cancer [RCV000101705]uncertain significance206000730160007301Humanname
8637411CV92637single nucleotide variantNM_177980.2(CDH26):c.27C>T (p.Pro9=)Malignant melanoma [RCV000072735]not provided205995875359958753Humanname
401860592CV2758536single nucleotide variantNM_177980.4(CDH26):c.16G>A (p.Gly6Arg)not specified [RCV004337628]likely benign205995874259958742Humanname
598169135CV3947429single nucleotide variantNM_177980.4(CDH26):c.26C>T (p.Pro9Leu)not specified [RCV005308363]uncertain significance205995875259958752Humanname
155932707CV2400077single nucleotide variantNM_177980.4(CDH26):c.43C>G (p.Leu15Val)not specified [RCV004246991]uncertain significance205995876959958769Humanname
597795449CV3641891single nucleotide variantNM_177980.4(CDH26):c.58T>C (p.Trp20Arg)not specified [RCV004903678]uncertain significance205995878459958784Humanname
156395988CV2326041single nucleotide variantNM_177980.4(CDH26):c.148C>G (p.Arg50Gly)not specified [RCV004176246]uncertain significance205997010359970103Humanname
329399772CV2467641single nucleotide variantNM_177980.4(CDH26):c.109C>A (p.Leu37Ile)not specified [RCV004287493]uncertain significance205996900659969006Humanname
401767922CV2678062single nucleotide variantNM_177980.4(CDH26):c.256A>G (p.Met86Val)not specified [RCV004296583]uncertain significance205997198659971986Humanname
405720746CV3296554single nucleotide variantNM_177980.4(CDH26):c.133A>G (p.Ile45Val)not specified [RCV004428103]uncertain significance205997008859970088Humanname
405720812CV3296563single nucleotide variantNM_177980.4(CDH26):c.232C>G (p.Leu78Val)not specified [RCV004428112]uncertain significance205997196259971962Humanname
407454998CV3422309single nucleotide variantNM_177980.4(CDH26):c.135C>G (p.Ile45Met)not specified [RCV004610100]uncertain significance205997009059970090Humanname
597795469CV3641898single nucleotide variantNM_177980.4(CDH26):c.139C>G (p.Gln47Glu)not specified [RCV004903685]uncertain significance205997009459970094Humanname
156232040CV2227649single nucleotide variantNM_177980.4(CDH26):c.307A>T (p.Ile103Phe)not specified [RCV004094053]uncertain significance205997203759972037Humanname
156023517CV2233461single nucleotide variantNM_177980.4(CDH26):c.655C>T (p.Arg219Trp)not specified [RCV004106085]uncertain significance205998475259984752Humanname
156276323CV2276777single nucleotide variantNM_177980.4(CDH26):c.877G>C (p.Val293Leu)not specified [RCV004140141]uncertain significance205998749259987492Humanname
401730890CV2686767single nucleotide variantNM_177980.4(CDH26):c.359G>A (p.Arg120His)not specified [RCV004301955]uncertain significance205997208959972089Humanname
401717586CV2714066single nucleotide variantNM_177980.4(CDH26):c.877G>A (p.Val293Met)not specified [RCV004315465]uncertain significance205998749259987492Humanname
401781997CV2719128single nucleotide variantNM_177980.4(CDH26):c.332A>G (p.His111Arg)not specified [RCV004324796]uncertain significance205997206259972062Humanname
401892456CV2781978single nucleotide variantNM_177980.4(CDH26):c.922G>T (p.Ala308Ser)not specified [RCV004357208]uncertain significance205998753759987537Humanname
405720844CV3296567single nucleotide variantNM_177980.4(CDH26):c.416G>T (p.Arg139Leu)not specified [RCV004428116]uncertain significance205998294559982945Humanname
405720854CV3296568single nucleotide variantNM_177980.4(CDH26):c.550A>G (p.Ile184Val)not specified [RCV004428117]uncertain significance205998464759984647Humanname
405720863CV3296569single nucleotide variantNM_177980.4(CDH26):c.764T>C (p.Leu255Pro)not specified [RCV004428118]uncertain significance205998505659985056Humanname
405720873CV3296570single nucleotide variantNM_177980.4(CDH26):c.944T>C (p.Ile315Thr)not specified [RCV004428119]uncertain significance205998755959987559Humanname
405720879CV3296571single nucleotide variantNM_177980.4(CDH26):c.998A>G (p.Asn333Ser)not specified [RCV004428120]uncertain significance205998761359987613Humanname
407454988CV3422304single nucleotide variantNM_177980.4(CDH26):c.326A>G (p.Glu109Gly)not specified [RCV004610095]uncertain significance205997205659972056Humanname
407454996CV3422308single nucleotide variantNM_177980.4(CDH26):c.831G>C (p.Gln277His)not specified [RCV004610099]uncertain significance205998512359985123Humanname
407455000CV3422310single nucleotide variantNM_177980.4(CDH26):c.389T>C (p.Phe130Ser)not specified [RCV004610101]uncertain significance205997211959972119Humanname
407455007CV3422313single nucleotide variantNM_177980.4(CDH26):c.373G>C (p.Glu125Gln)not specified [RCV004610104]uncertain significance205997210359972103Humanname
597795446CV3641890single nucleotide variantNM_177980.4(CDH26):c.758C>T (p.Pro253Leu)not specified [RCV004903677]uncertain significance205998505059985050Humanname
598169025CV3947412single nucleotide variantNM_177980.4(CDH26):c.863G>A (p.Arg288Gln)not specified [RCV005308348]likely benign205998747859987478Humanname
598169035CV3947413single nucleotide variantNM_177980.4(CDH26):c.733A>G (p.Ile245Val)not specified [RCV005308349]uncertain significance205998502559985025Humanname
598169060CV3947418single nucleotide variantNM_177980.4(CDH26):c.378G>A (p.Met126Ile)not specified [RCV005308352]uncertain significance205997210859972108Humanname
598169079CV3947421single nucleotide variantNM_177980.4(CDH26):c.744G>C (p.Arg248Ser)not specified [RCV005308355]uncertain significance205998503659985036Humanname
598169103CV3947424single nucleotide variantNM_177980.4(CDH26):c.533A>C (p.Gln178Pro)not specified [RCV005308358]uncertain significance205998306259983062Humanname
598169125CV3947427single nucleotide variantNM_177980.4(CDH26):c.347T>C (p.Ile116Thr)not specified [RCV005308361]uncertain significance205997207759972077Humanname
156374442CV2198457single nucleotide variantNM_177980.4(CDH26):c.1284A>C (p.Arg428Ser)not specified [RCV004081985]uncertain significance205999237859992378Humanname
155960411CV2204206single nucleotide variantNM_177980.4(CDH26):c.2221G>C (p.Ala741Pro)not specified [RCV004077002]uncertain significance206000671360006713Humanname
156224300CV2219323single nucleotide variantNM_177980.4(CDH26):c.2090G>C (p.Gly697Ala)not specified [RCV004095170]uncertain significance205999965659999656Humanname
156382846CV2223660single nucleotide variantNM_177980.4(CDH26):c.1705C>T (p.Arg569Cys)not specified [RCV004093783]uncertain significance205999587159995871Humanname
156188706CV2226786single nucleotide variantNM_177980.4(CDH26):c.2480A>G (p.Glu827Gly)not specified [RCV004102000]uncertain significance206001271160012711Humanname
156244893CV2231640single nucleotide variantNM_177980.4(CDH26):c.2276T>C (p.Met759Thr)not specified [RCV004098211]uncertain significance206000676860006768Humanname
156184419CV2239193single nucleotide variantNM_177980.4(CDH26):c.1874T>C (p.Phe625Ser)not specified [RCV004112175]uncertain significance205999604059996040Humanname
155919531CV2279436single nucleotide variantNM_177980.4(CDH26):c.1996G>A (p.Glu666Lys)not specified [RCV004141976]uncertain significance205999673859996738Humanname
155992580CV2281225single nucleotide variantNM_177980.4(CDH26):c.1193C>T (p.Pro398Leu)not specified [RCV004147474]uncertain significance205998907359989073Humanname
156075090CV2281494single nucleotide variantNM_177980.4(CDH26):c.1157A>G (p.Gln386Arg)not specified [RCV004153811]uncertain significance205998903759989037Humanname
156278936CV2285008single nucleotide variantNM_177980.4(CDH26):c.1654G>A (p.Gly552Arg)not specified [RCV004143437]uncertain significance205999447759994477Humanname
155940388CV2294070single nucleotide variantNM_177980.4(CDH26):c.1340T>C (p.Val447Ala)not specified [RCV004149449]likely benign205999243459992434Humanname
155999404CV2296192single nucleotide variantNM_177980.4(CDH26):c.1397A>G (p.Tyr466Cys)not specified [RCV004154112]uncertain significance205999249159992491Humanname
156083514CV2298995single nucleotide variantNM_177980.4(CDH26):c.1999A>G (p.Ser667Gly)not specified [RCV004158520]uncertain significance205999674159996741Humanname
156039024CV2313698single nucleotide variantNM_177980.4(CDH26):c.2069C>G (p.Ala690Gly)not specified [RCV004157615]uncertain significance205999963559999635Humanname
156283361CV2318846single nucleotide variantNM_177980.4(CDH26):c.2444G>T (p.Gly815Val)not specified [RCV004175755]uncertain significance206001267560012675Humanname
156066936CV2356573single nucleotide variantNM_177980.4(CDH26):c.2422C>T (p.Pro808Ser)not specified [RCV004201940]uncertain significance206001265360012653Humanname
156286725CV2360949single nucleotide variantNM_177980.4(CDH26):c.1168G>A (p.Ala390Thr)not specified [RCV004215760]uncertain significance205998904859989048Humanname
156085695CV2366219single nucleotide variantNM_177980.4(CDH26):c.1207G>T (p.Val403Phe)not specified [RCV004210237]uncertain significance205998908759989087Humanname
156387357CV2372720single nucleotide variantNM_177980.4(CDH26):c.1790G>T (p.Cys597Phe)not specified [RCV004221912]uncertain significance205999595659995956Humanname
156140551CV2383624single nucleotide variantNM_177980.4(CDH26):c.1815G>C (p.Glu605Asp)not specified [RCV004229515]uncertain significance205999598159995981Humanname
329368403CV2428007single nucleotide variantNM_177980.4(CDH26):c.2332G>A (p.Gly778Ser)not specified [RCV004254386]likely benign206001256360012563Humanname
401741892CV2676549single nucleotide variantNM_177980.4(CDH26):c.2133G>T (p.Gln711His)not specified [RCV004288737]uncertain significance206000137860001378Humanname
401742995CV2694029single nucleotide variantNM_177980.4(CDH26):c.1118C>T (p.Pro373Leu)not specified [RCV004302472]uncertain significance205998899859988998Humanname
401735106CV2699165single nucleotide variantNM_177980.4(CDH26):c.1488C>A (p.Asn496Lys)not specified [RCV004303665]uncertain significance205999431159994311Humanname
401777675CV2718296single nucleotide variantNM_177980.4(CDH26):c.2356G>A (p.Glu786Lys)not specified [RCV004318136]uncertain significance206001258760012587Humanname
401880563CV2763089single nucleotide variantNM_177980.4(CDH26):c.2410C>G (p.Gln804Glu)not specified [RCV004336139]uncertain significance206001264160012641Humanname
401861217CV2769580single nucleotide variantNM_177980.4(CDH26):c.1894C>G (p.Leu632Val)not specified [RCV004351227]uncertain significance205999663659996636Humanname
401870111CV2772621single nucleotide variantNM_177980.4(CDH26):c.1879G>A (p.Ala627Thr)not specified [RCV004355371]uncertain significance205999604559996045Humanname
405720713CV3296550single nucleotide variantNM_177980.4(CDH26):c.1024C>G (p.Pro342Ala)not specified [RCV004428099]uncertain significance205998890459988904Humanname
405720723CV3296551single nucleotide variantNM_177980.4(CDH26):c.1049C>T (p.Ala350Val)not specified [RCV004428100]likely benign205998892959988929Humanname
405720728CV3296552single nucleotide variantNM_177980.4(CDH26):c.1204A>T (p.Ile402Phe)not specified [RCV004428101]uncertain significance205998908459989084Humanname
405720739CV3296553single nucleotide variantNM_177980.4(CDH26):c.1216G>A (p.Glu406Lys)not specified [RCV004428102]likely benign205998909659989096Humanname
405720752CV3296555single nucleotide variantNM_177980.4(CDH26):c.1351G>A (p.Val451Met)not specified [RCV004428104]uncertain significance205999244559992445Humanname
405720760CV3296556single nucleotide variantNM_177980.4(CDH26):c.1369G>A (p.Glu457Lys)not specified [RCV004428105]uncertain significance205999246359992463Humanname
405720767CV3296557single nucleotide variantNM_177980.4(CDH26):c.1372T>A (p.Ser458Thr)not specified [RCV004428106]uncertain significance205999246659992466Humanname
405720774CV3296558single nucleotide variantNM_177980.4(CDH26):c.1652T>C (p.Leu551Ser)not specified [RCV004428107]uncertain significance205999447559994475Humanname
405720782CV3296559single nucleotide variantNM_177980.4(CDH26):c.1675G>C (p.Val559Leu)not specified [RCV004428108]uncertain significance205999584159995841Humanname
405720790CV3296560single nucleotide variantNM_177980.4(CDH26):c.1786C>G (p.Pro596Ala)not specified [RCV004428109]uncertain significance205999595259995952Humanname
405720796CV3296561single nucleotide variantNM_177980.4(CDH26):c.1793C>G (p.Ala598Gly)not specified [RCV004428110]uncertain significance205999595959995959Humanname
405720803CV3296562single nucleotide variantNM_177980.4(CDH26):c.2263G>A (p.Val755Met)not specified [RCV004428111]uncertain significance206000675560006755Humanname
405720820CV3296564single nucleotide variantNM_177980.4(CDH26):c.2355C>A (p.Ser785Arg)not specified [RCV004428113]uncertain significance206001258660012586Humanname
405720828CV3296565single nucleotide variantNM_177980.4(CDH26):c.2407G>A (p.Glu803Lys)not specified [RCV004428114]uncertain significance206001263860012638Humanname
405720836CV3296566single nucleotide variantNM_177980.4(CDH26):c.2485G>A (p.Gly829Ser)not specified [RCV004428115]uncertain significance206001271660012716Humanname
407454990CV3422305single nucleotide variantNM_177980.4(CDH26):c.1321G>A (p.Val441Ile)not specified [RCV004610096]uncertain significance205999241559992415Humanname
407454992CV3422306single nucleotide variantNM_177980.4(CDH26):c.1153G>A (p.Val385Met)not specified [RCV004610097]uncertain significance205998903359989033Humanname
407455002CV3422311single nucleotide variantNM_177980.4(CDH26):c.2207T>C (p.Ile736Thr)not specified [RCV004610102]uncertain significance206000285360002853Humanname
407455005CV3422312single nucleotide variantNM_177980.4(CDH26):c.1982T>A (p.Val661Asp)not specified [RCV004610103]uncertain significance205999672459996724Humanname
597795452CV3641892single nucleotide variantNM_177980.4(CDH26):c.1622C>T (p.Thr541Ile)not specified [RCV004903679]uncertain significance205999444559994445Humanname
597795455CV3641893single nucleotide variantNM_177980.4(CDH26):c.2347G>A (p.Val783Ile)not specified [RCV004903680]uncertain significance206001257860012578Humanname
597795458CV3641894single nucleotide variantNM_177980.4(CDH26):c.1870G>T (p.Ala624Ser)not specified [RCV004903681]uncertain significance205999603659996036Humanname
597795461CV3641895single nucleotide variantNM_177980.4(CDH26):c.1128G>C (p.Lys376Asn)not specified [RCV004903682]uncertain significance205998900859989008Humanname
597795467CV3641897single nucleotide variantNM_177980.4(CDH26):c.2224T>A (p.Tyr742Asn)not specified [RCV004903684]uncertain significance206000671660006716Humanname
597795472CV3641899single nucleotide variantNM_177980.4(CDH26):c.1325A>G (p.Asp442Gly)not specified [RCV004903686]uncertain significance205999241959992419Humanname
597795475CV3641900single nucleotide variantNM_177980.4(CDH26):c.1103G>A (p.Arg368Lys)not specified [RCV004903687]uncertain significance205998898359988983Humanname
597795478CV3641901single nucleotide variantNM_177980.4(CDH26):c.1769T>C (p.Val590Ala)not specified [RCV004903688]uncertain significance205999593559995935Humanname
597795481CV3641902single nucleotide variantNM_177980.4(CDH26):c.1972C>A (p.Gln658Lys)not specified [RCV004903689]uncertain significance205999671459996714Humanname
597795484CV3641903single nucleotide variantNM_177980.4(CDH26):c.1285T>C (p.Tyr429His)not specified [RCV004903690]uncertain significance205999237959992379Humanname
597795487CV3641904single nucleotide variantNM_177980.4(CDH26):c.1298A>C (p.His433Pro)not specified [RCV004903691]uncertain significance205999239259992392Humanname
598168994CV3947407single nucleotide variantNM_177980.4(CDH26):c.1513C>T (p.Arg505Cys)not specified [RCV005308343]uncertain significance205999433659994336Humanname
598169001CV3947408single nucleotide variantNM_177980.4(CDH26):c.1994C>T (p.Ala665Val)not specified [RCV005308344]uncertain significance205999673659996736Humanname
598169009CV3947409single nucleotide variantNM_177980.4(CDH26):c.2084C>T (p.Thr695Met)not specified [RCV005308345]uncertain significance205999965059999650Humanname
598169019CV3947411single nucleotide variantNM_177980.4(CDH26):c.1418T>C (p.Val473Ala)not specified [RCV005308347]uncertain significance205999251259992512Humanname
598229670CV3947414single nucleotide variantNM_177980.4(CDH26):c.1246G>A (p.Gly416Arg)not specified [RCV005319266]uncertain significance205998912659989126Humanname
598169042CV3947415single nucleotide variantNM_177980.4(CDH26):c.1493C>G (p.Pro498Arg)not specified [RCV005308350]uncertain significance205999431659994316Humanname
598229676CV3947416single nucleotide variantNM_177980.4(CDH26):c.1867G>T (p.Ala623Ser)not specified [RCV005319267]uncertain significance205999603359996033Humanname
598169051CV3947417single nucleotide variantNM_177980.4(CDH26):c.1077T>G (p.Asn359Lys)not specified [RCV005308351]uncertain significance205998895759988957Humanname
598169072CV3947420single nucleotide variantNM_177980.4(CDH26):c.2398G>A (p.Ala800Thr)not specified [RCV005308354]likely benign206001262960012629Humanname
598169088CV3947422single nucleotide variantNM_177980.4(CDH26):c.1561G>A (p.Glu521Lys)not specified [RCV005308356]uncertain significance205999438459994384Humanname
598169096CV3947423single nucleotide variantNM_177980.4(CDH26):c.2119T>C (p.Ser707Pro)not specified [RCV005308357]uncertain significance206000136460001364Humanname
598169112CV3947425single nucleotide variantNM_177980.4(CDH26):c.1531G>A (p.Glu511Lys)not specified [RCV005308359]uncertain significance205999435459994354Humanname
598169119CV3947426single nucleotide variantNM_177980.4(CDH26):c.2326G>T (p.Asp776Tyr)not specified [RCV005308360]uncertain significance206001255760012557Humanname
598169130CV3947428single nucleotide variantNM_177980.4(CDH26):c.2278G>C (p.Ala760Pro)not specified [RCV005308362]uncertain significance206000677060006770Humanname
598169146CV3947431single nucleotide variantNM_177980.4(CDH26):c.1762C>G (p.Gln588Glu)not specified [RCV005308365]uncertain significance205999592859995928Humanname