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Variants search result for Homo sapiens
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88 records found for search term Sema4c
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
598212700CV3903991single nucleotide variantNM_017789.5(SEMA4C):c.8C>T (p.Pro3Leu)not specified [RCV005270999]uncertain significance29686787996867879Humanname
405727721CV3317357single nucleotide variantNM_017789.5(SEMA4C):c.17C>T (p.Ala6Val)not specified [RCV004450619]uncertain significance29686787096867870Humanname
401760421CV2718834single nucleotide variantNM_017789.5(SEMA4C):c.67G>A (p.Val23Met)not specified [RCV004328578]uncertain significance29686782096867820Humanname
598212694CV3903990single nucleotide variantNM_017789.5(SEMA4C):c.56T>C (p.Ile19Thr)not specified [RCV005270998]uncertain significance29686783196867831Humanname
155982691CV2233213single nucleotide variantNM_017789.5(SEMA4C):c.131G>A (p.Arg44Gln)not specified [RCV004105607]uncertain significance29686641096866410Humanname
156067684CV2381106single nucleotide variantNM_017789.5(SEMA4C):c.170C>T (p.Thr57Met)not specified [RCV004225138]uncertain significance29686637196866371Humanname
401737725CV2679959single nucleotide variantNM_017789.5(SEMA4C):c.176C>T (p.Thr59Met)not specified [RCV004284237]uncertain significance29686636596866365Humanname
401752330CV2682783single nucleotide variantNM_017789.5(SEMA4C):c.205G>A (p.Ala69Thr)not specified [RCV004281756]uncertain significance29686633696866336Humanname
401894039CV2774385single nucleotide variantNM_017789.5(SEMA4C):c.233T>C (p.Met78Thr)not specified [RCV004347727]uncertain significance29686630896866308Humanname
597736283CV3601968single nucleotide variantNM_017789.5(SEMA4C):c.187G>A (p.Gly63Arg)not specified [RCV004863803]uncertain significance29686635496866354Humanname
155996619CV2288529single nucleotide variantNM_017789.5(SEMA4C):c.592C>T (p.His198Tyr)not specified [RCV004152061]uncertain significance29686524696865246Humanname
156395401CV2329172single nucleotide variantNM_017789.5(SEMA4C):c.826A>T (p.Thr276Ser)not specified [RCV004173926]uncertain significance29686484196864841Humanname
156308681CV2341663single nucleotide variantNM_017789.5(SEMA4C):c.653C>G (p.Ser218Cys)not specified [RCV004182587]uncertain significance29686509796865097Humanname
156222862CV2344001single nucleotide variantNM_017789.5(SEMA4C):c.325G>A (p.Glu109Lys)not specified [RCV004195618]uncertain significance29686576196865761Humanname
401770377CV2715161single nucleotide variantNM_017789.5(SEMA4C):c.895G>A (p.Ala299Thr)not specified [RCV004324518]uncertain significance29686477296864772Humanname
401873440CV2761467single nucleotide variantNM_017789.5(SEMA4C):c.985A>G (p.Ile329Val)not specified [RCV004334641]likely benign29686436096864360Humanname
401866164CV2762550single nucleotide variantNM_017789.5(SEMA4C):c.929A>C (p.Asn310Thr)not specified [RCV004338083]uncertain significance29686473896864738Humanname
405727795CV3317366single nucleotide variantNM_017789.5(SEMA4C):c.725G>A (p.Arg242Gln)not specified [RCV004450628]uncertain significance29686502596865025Humanname
405727802CV3317367single nucleotide variantNM_017789.5(SEMA4C):c.751G>A (p.Glu251Lys)not specified [RCV004450629]uncertain significance29686499996864999Humanname
405727811CV3317368single nucleotide variantNM_017789.5(SEMA4C):c.766C>T (p.Arg256Cys)not specified [RCV004450630]uncertain significance29686498496864984Humanname
405727819CV3317369single nucleotide variantNM_017789.5(SEMA4C):c.863C>T (p.Pro288Leu)not specified [RCV004450631]uncertain significance29686480496864804Humanname
407492306CV3473414single nucleotide variantNM_017789.5(SEMA4C):c.724C>T (p.Arg242Trp)not specified [RCV004667082]uncertain significance29686502696865026Humanname
407477857CV3473416single nucleotide variantNM_017789.5(SEMA4C):c.502G>A (p.Ala168Thr)not specified [RCV004663797]likely benign29686545696865456Humanname
597736322CV3601975single nucleotide variantNM_017789.5(SEMA4C):c.794T>C (p.Met265Thr)not specified [RCV004863810]uncertain significance29686487396864873Humanname
597736333CV3601977single nucleotide variantNM_017789.5(SEMA4C):c.431C>A (p.Thr144Asn)not specified [RCV004863812]uncertain significance29686552796865527Humanname
598212686CV3903989single nucleotide variantNM_017789.5(SEMA4C):c.689G>A (p.Gly230Glu)not specified [RCV005270997]uncertain significance29686506196865061Humanname
8630489CV85644single nucleotide variantNM_017789.4(SEMA4C):c.920C>T (p.Ser307Phe)Malignant melanoma [RCV000065727]not provided29686474796864747Humanname
156244592CV2231616single nucleotide variantNM_017789.5(SEMA4C):c.1240G>A (p.Val414Met)not specified [RCV004096655]uncertain significance29686401696864016Humanname
155921093CV2240469single nucleotide variantNM_017789.5(SEMA4C):c.2203G>A (p.Gly735Ser)not specified [RCV004117349]uncertain significance29686092596860925Humanname
156297642CV2246889single nucleotide variantNM_017789.5(SEMA4C):c.1266C>A (p.His422Gln)not specified [RCV004112693]uncertain significance29686399096863990Humanname
156148778CV2265300single nucleotide variantNM_017789.5(SEMA4C):c.1778G>A (p.Arg593Gln)not specified [RCV004128192]uncertain significance29686135096861350Humanname
155984236CV2273164single nucleotide variantNM_017789.5(SEMA4C):c.2152C>G (p.Pro718Ala)not specified [RCV004137798]uncertain significance29686097696860976Humanname
156245807CV2310438single nucleotide variantNM_017789.5(SEMA4C):c.2098G>A (p.Ala700Thr)not specified [RCV004163472]uncertain significance29686103096861030Humanname
156058185CV2322907single nucleotide variantNM_017789.5(SEMA4C):c.1473G>C (p.Gln491His)not specified [RCV004185358]uncertain significance29686186596861865Humanname
156160682CV2323381single nucleotide variantNM_017789.5(SEMA4C):c.1465C>T (p.Arg489Cys)not specified [RCV004171779]uncertain significance29686187396861873Humanname
156036669CV2332468single nucleotide variantNM_017789.5(SEMA4C):c.2398G>A (p.Gly800Arg)not specified [RCV004196194]uncertain significance29686073096860730Humanname
156072042CV2365360single nucleotide variantNM_017789.5(SEMA4C):c.1727C>G (p.Pro576Arg)not specified [RCV004209445]uncertain significance29686140196861401Humanname
156385246CV2368227single nucleotide variantNM_017789.5(SEMA4C):c.1679C>A (p.Pro560His)not specified [RCV004219024]uncertain significance29686144996861449Humanname
156320247CV2400348single nucleotide variantNM_017789.5(SEMA4C):c.1106C>T (p.Ser369Leu)not specified [RCV004244403]uncertain significance29686423996864239Humanname
329399787CV2444183single nucleotide variantNM_017789.5(SEMA4C):c.1016G>A (p.Arg339Gln)not specified [RCV004260916]uncertain significance29686432996864329Humanname
329377751CV2450039single nucleotide variantNM_017789.5(SEMA4C):c.1759C>T (p.Arg587Cys)not specified [RCV004269090]uncertain significance29686136996861369Humanname
329386783CV2452522single nucleotide variantNM_017789.5(SEMA4C):c.2225C>G (p.Ser742Cys)not specified [RCV004273116]uncertain significance29686090396860903Humanname
329372103CV2455047single nucleotide variantNM_017789.5(SEMA4C):c.1643G>C (p.Gly548Ala)not specified [RCV004272301]uncertain significance29686160896861608Humanname
401773318CV2698171single nucleotide variantNM_017789.5(SEMA4C):c.1282G>A (p.Val428Ile)not specified [RCV004304741]uncertain significance29686397496863974Humanname
401718642CV2704719single nucleotide variantNM_017789.5(SEMA4C):c.1075A>C (p.Thr359Pro)not specified [RCV004307322]uncertain significance29686427096864270Humanname
401721893CV2710221single nucleotide variantNM_017789.5(SEMA4C):c.1457C>T (p.Ala486Val)not specified [RCV004317120]uncertain significance29686188196861881Humanname
401783794CV2720439single nucleotide variantNM_017789.5(SEMA4C):c.1547A>G (p.Tyr516Cys)not specified [RCV004327864]uncertain significance29686179196861791Humanname
401861098CV2758749single nucleotide variantNM_017789.5(SEMA4C):c.2288C>T (p.Pro763Leu)not specified [RCV004337808]uncertain significance29686084096860840Humanname
401885482CV2759714single nucleotide variantNM_017789.5(SEMA4C):c.2066G>A (p.Arg689Gln)not specified [RCV004342766]uncertain significance29686106296861062Humanname
401893531CV2765249single nucleotide variantNM_017789.5(SEMA4C):c.1573C>T (p.Arg525Cys)not specified [RCV004339773]uncertain significance29686176596861765Humanname
401885323CV2768085single nucleotide variantNM_017789.5(SEMA4C):c.2344C>T (p.Arg782Trp)not specified [RCV004348317]uncertain significance29686078496860784Humanname
401880308CV2783165single nucleotide variantNM_017789.5(SEMA4C):c.2072G>A (p.Arg691Gln)not specified [RCV004363512]uncertain significance29686105696861056Humanname
401899129CV2783681single nucleotide variantNM_017789.5(SEMA4C):c.1126C>T (p.Arg376Trp)not specified [RCV004360612]uncertain significance29686413096864130Humanname
405727699CV3317355single nucleotide variantNM_017789.5(SEMA4C):c.1501A>G (p.Met501Val)not specified [RCV004450617]likely benign29686183796861837Humanname
405727712CV3317356single nucleotide variantNM_017789.5(SEMA4C):c.1760G>A (p.Arg587His)not specified [RCV004450618]uncertain significance29686136896861368Humanname
405727730CV3317358single nucleotide variantNM_017789.5(SEMA4C):c.1807T>C (p.Phe603Leu)not specified [RCV004450620]uncertain significance29686132196861321Humanname
405727741CV3317359single nucleotide variantNM_017789.5(SEMA4C):c.1808T>A (p.Phe603Tyr)not specified [RCV004450621]uncertain significance29686132096861320Humanname
405727750CV3317360single nucleotide variantNM_017789.5(SEMA4C):c.1880G>A (p.Cys627Tyr)not specified [RCV004450622]uncertain significance29686124896861248Humanname
405727758CV3317361single nucleotide variantNM_017789.5(SEMA4C):c.2152C>A (p.Pro718Thr)not specified [RCV004450623]uncertain significance29686097696860976Humanname
405727772CV3317363single nucleotide variantNM_017789.5(SEMA4C):c.2252G>A (p.Arg751Gln)not specified [RCV004450625]uncertain significance29686087696860876Humanname
405727778CV3317364single nucleotide variantNM_017789.5(SEMA4C):c.2252G>C (p.Arg751Pro)not specified [RCV004450626]uncertain significance29686087696860876Humanname
405727787CV3317365single nucleotide variantNM_017789.5(SEMA4C):c.2432A>G (p.Asp811Gly)not specified [RCV004450627]uncertain significance29686069696860696Humanname
407477839CV3473411single nucleotide variantNM_017789.5(SEMA4C):c.2339G>C (p.Gly780Ala)not specified [RCV004663794]uncertain significance29686078996860789Humanname
407477845CV3473412single nucleotide variantNM_017789.5(SEMA4C):c.2161C>T (p.Arg721Trp)not specified [RCV004663795]uncertain significance29686096796860967Humanname
407492303CV3473413single nucleotide variantNM_017789.5(SEMA4C):c.2473G>A (p.Asp825Asn)not specified [RCV004667081]uncertain significance29686065596860655Humanname
407477852CV3473415single nucleotide variantNM_017789.5(SEMA4C):c.2263G>A (p.Gly755Ser)not specified [RCV004663796]uncertain significance29686086596860865Humanname
597736288CV3601969single nucleotide variantNM_017789.5(SEMA4C):c.2485G>A (p.Glu829Lys)not specified [RCV004863804]uncertain significance29686064396860643Humanname
597736292CV3601970single nucleotide variantNM_017789.5(SEMA4C):c.1538G>A (p.Arg513Gln)not specified [RCV004863805]uncertain significance29686180096861800Humanname
597736298CV3601971single nucleotide variantNM_017789.5(SEMA4C):c.1229G>A (p.Arg410His)not specified [RCV004863806]uncertain significance29686402796864027Humanname
597736304CV3601972single nucleotide variantNM_017789.5(SEMA4C):c.2429C>T (p.Ala810Val)not specified [RCV004863807]uncertain significance29686069996860699Humanname
597736309CV3601973single nucleotide variantNM_017789.5(SEMA4C):c.1652A>G (p.Asn551Ser)not specified [RCV004863808]uncertain significance29686159996861599Humanname
597736315CV3601974single nucleotide variantNM_017789.5(SEMA4C):c.1520C>T (p.Ala507Val)not specified [RCV004863809]uncertain significance29686181896861818Humanname
597736327CV3601976single nucleotide variantNM_017789.5(SEMA4C):c.1904G>A (p.Arg635Gln)not specified [RCV004863811]uncertain significance29686122496861224Humanname
598212613CV3903978single nucleotide variantNM_017789.5(SEMA4C):c.2279C>T (p.Ser760Leu)not specified [RCV005270986]uncertain significance29686084996860849Humanname
598212620CV3903979single nucleotide variantNM_017789.5(SEMA4C):c.2404C>T (p.Leu802Phe)not specified [RCV005270987]uncertain significance29686072496860724Humanname
598212626CV3903980single nucleotide variantNM_017789.5(SEMA4C):c.1657C>T (p.Arg553Cys)not specified [RCV005270988]uncertain significance29686159496861594Humanname
598212632CV3903981single nucleotide variantNM_017789.5(SEMA4C):c.1372G>A (p.Val458Ile)not specified [RCV005270989]uncertain significance29686375396863753Humanname
598212638CV3903982single nucleotide variantNM_017789.5(SEMA4C):c.1654C>T (p.Leu552Phe)not specified [RCV005270990]likely benign29686159796861597Humanname
598212650CV3903984single nucleotide variantNM_017789.5(SEMA4C):c.2156C>G (p.Pro719Arg)not specified [RCV005270992]uncertain significance29686097296860972Humanname
598212658CV3903985single nucleotide variantNM_017789.5(SEMA4C):c.1658G>A (p.Arg553His)not specified [RCV005270993]uncertain significance29686159396861593Humanname
598212664CV3903986single nucleotide variantNM_017789.5(SEMA4C):c.1790C>T (p.Ala597Val)not specified [RCV005270994]uncertain significance29686133896861338Humanname
598212671CV3903987single nucleotide variantNM_017789.5(SEMA4C):c.1247A>G (p.Lys416Arg)not specified [RCV005270995]uncertain significance29686400996864009Humanname
598212679CV3903988single nucleotide variantNM_017789.5(SEMA4C):c.1067A>C (p.Asp356Ala)not specified [RCV005270996]uncertain significance29686427896864278Humanname
598212708CV3903992single nucleotide variantNM_017789.5(SEMA4C):c.2441G>C (p.Arg814Thr)not specified [RCV005271000]uncertain significance29686068796860687Humanname
598212715CV3903993single nucleotide variantNM_017789.5(SEMA4C):c.1371G>C (p.Trp457Cys)not specified [RCV005271001]uncertain significance29686375496863754Humanname
598212724CV3903995single nucleotide variantNM_017789.5(SEMA4C):c.1818T>A (p.Asp606Glu)not specified [RCV005271003]uncertain significance29686131096861310Humanname
8625434CV80557single nucleotide variantNM_017789.4(SEMA4C):c.1558A>G (p.Ser520Gly)Malignant melanoma [RCV000060634]not provided29686178096861780Humanname
8630488CV85643single nucleotide variantNM_017789.4(SEMA4C):c.1219C>T (p.Arg407Trp)Malignant melanoma [RCV000065726]not provided29686403796864037Humanname