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Variants search result for Homo sapiens
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110 records found for search term Sema6a
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15132415CV744183single nucleotide variantNM_020796.5(SEMA6A):c.219-3T>Cnot provided [RCV000897952]likely benign5116497390116497390Humanname
8580271CV114701single nucleotide variantNM_020796.4(SEMA6A):c.-38-17728T>GLung cancer [RCV000095224]uncertain significance5116522710116522710Humanname
156384995CV2371667single nucleotide variantNM_020796.5(SEMA6A):c.14C>A (p.Ala5Asp)not specified [RCV004216905]uncertain significance5116504931116504931Humanname
15156304CV721166single nucleotide variantNM_020796.5(SEMA6A):c.198A>G (p.Gly66=)not provided [RCV000880599]benign5116502230116502230Humanname
15145466CV749148single nucleotide variantNM_020796.5(SEMA6A):c.270T>C (p.Tyr90=)not provided [RCV000922547]benign5116497336116497336Humanname
405728690CV3317464single nucleotide variantNM_020796.5(SEMA6A):c.50G>C (p.Gly17Ala)not specified [RCV004450726]uncertain significance5116504895116504895Humanname
15145207CV709574single nucleotide variantNM_020796.5(SEMA6A):c.480C>T (p.Ser160=)not provided [RCV000966956]benign5116491795116491795Humanname
15114278CV709575single nucleotide variantNM_020796.5(SEMA6A):c.465C>T (p.Phe155=)not provided [RCV000961646]benign5116491810116491810Humanname
15163084CV734809single nucleotide variantNM_020796.5(SEMA6A):c.720A>G (p.Ala240=)not provided [RCV000903695]benign5116488132116488132Humanname
156398792CV2194790single nucleotide variantNM_020796.5(SEMA6A):c.163A>G (p.Arg55Gly)not specified [RCV004075336]uncertain significance5116502265116502265Humanname
155952946CV2264289single nucleotide variantNM_020796.5(SEMA6A):c.192G>A (p.Met64Ile)not specified [RCV004138212]uncertain significance5116502236116502236Humanname
156167288CV2270475single nucleotide variantNM_020796.5(SEMA6A):c.202C>G (p.Leu68Val)not specified [RCV004137439]uncertain significance5116502226116502226Humanname
155989168CV2352169single nucleotide variantNM_020796.5(SEMA6A):c.186G>A (p.Met62Ile)not specified [RCV004200658]uncertain significance5116502242116502242Humanname
329358439CV2425256single nucleotide variantNM_020796.5(SEMA6A):c.143G>A (p.Arg48Gln)not specified [RCV004250928]uncertain significance5116502285116502285Humanname
401914991CV2827949single nucleotide variantNM_020796.5(SEMA6A):c.1692T>C (p.Gly564=)not provided [RCV003428585]likely benign5116475561116475561Humanname
597736680CV3602060single nucleotide variantNM_020796.5(SEMA6A):c.284T>G (p.Leu95Arg)not specified [RCV004863888]uncertain significance5116496309116496309Humanname
597736700CV3602065single nucleotide variantNM_020796.5(SEMA6A):c.257C>T (p.Thr86Met)not specified [RCV004863892]uncertain significance5116497349116497349Humanname
597736712CV3602067single nucleotide variantNM_020796.5(SEMA6A):c.149C>A (p.Thr50Asn)not specified [RCV004863894]uncertain significance5116502279116502279Humanname
598224052CV3904064single nucleotide variantNM_020796.5(SEMA6A):c.286A>T (p.Thr96Ser)not specified [RCV005273141]uncertain significance5116496307116496307Humanname
15133318CV709573single nucleotide variantNM_020796.5(SEMA6A):c.1623C>G (p.Ala541=)not provided [RCV000964931]likely benign5116477872116477872Humanname
156050685CV2269304single nucleotide variantNM_020796.5(SEMA6A):c.307G>A (p.Asp103Asn)not specified [RCV004130709]uncertain significance5116496286116496286Humanname
156244313CV2313084single nucleotide variantNM_020796.5(SEMA6A):c.473A>C (p.Glu158Ala)not specified [RCV004161357]uncertain significance5116491802116491802Humanname
156336958CV2360851single nucleotide variantNM_020796.5(SEMA6A):c.686G>C (p.Gly229Ala)not specified [RCV004213622]uncertain significance5116488166116488166Humanname
155906110CV2393877single nucleotide variantNM_020796.5(SEMA6A):c.385G>A (p.Asp129Asn)not specified [RCV004233700]uncertain significance5116495472116495472Humanname
401772398CV2687513single nucleotide variantNM_020796.5(SEMA6A):c.959A>G (p.Asn320Ser)not specified [RCV004300746]uncertain significance5116486752116486752Humanname
401896145CV2773662single nucleotide variantNM_020796.5(SEMA6A):c.915C>G (p.Ile305Met)not specified [RCV004356350]uncertain significance5116486796116486796Humanname
405728697CV3317465single nucleotide variantNM_020796.5(SEMA6A):c.709A>G (p.Arg237Gly)not specified [RCV004450727]uncertain significance5116488143116488143Humanname
405728706CV3317466single nucleotide variantNM_020796.5(SEMA6A):c.865T>G (p.Ser289Ala)not specified [RCV004450728]uncertain significance5116486846116486846Humanname
405728720CV3317467single nucleotide variantNM_020796.5(SEMA6A):c.893C>A (p.Ala298Glu)not specified [RCV004450729]uncertain significance5116486818116486818Humanname
405728731CV3317468single nucleotide variantNM_020796.5(SEMA6A):c.919G>A (p.Gly307Arg)not specified [RCV004450730]uncertain significance5116486792116486792Humanname
597736623CV3602048single nucleotide variantNM_020796.5(SEMA6A):c.716T>C (p.Ile239Thr)not specified [RCV004863877]uncertain significance5116488136116488136Humanname
597736643CV3602052single nucleotide variantNM_020796.5(SEMA6A):c.728A>G (p.Tyr243Cys)not specified [RCV004863881]uncertain significance5116488124116488124Humanname
597736670CV3602058single nucleotide variantNM_020796.5(SEMA6A):c.536A>G (p.Asp179Gly)not specified [RCV004863886]uncertain significance5116489007116489007Humanname
597736685CV3602061single nucleotide variantNM_020796.5(SEMA6A):c.731A>T (p.Asn244Ile)not specified [RCV004863889]uncertain significance5116488121116488121Humanname
597736690CV3602062single nucleotide variantNM_020796.5(SEMA6A):c.460C>A (p.Pro154Thr)not specified [RCV004863890]uncertain significance5116491815116491815Humanname
597736727CV3602070single nucleotide variantNM_020796.5(SEMA6A):c.754C>T (p.Pro252Ser)not specified [RCV004863897]uncertain significance5116486957116486957Humanname
598224058CV3904065single nucleotide variantNM_020796.5(SEMA6A):c.896T>C (p.Val299Ala)not specified [RCV005273142]uncertain significance5116486815116486815Humanname
598224098CV3904071single nucleotide variantNM_020796.5(SEMA6A):c.461C>T (p.Pro154Leu)not specified [RCV005273148]uncertain significance5116491814116491814Humanname
156380740CV2208371single nucleotide variantNM_020796.5(SEMA6A):c.1772C>T (p.Ser591Leu)not specified [RCV004088803]uncertain significance5116467705116467705Humanname
156119359CV2228892single nucleotide variantNM_020796.5(SEMA6A):c.2489T>C (p.Val830Ala)not specified [RCV004095122]uncertain significance5116447217116447217Humanname
156229593CV2234984single nucleotide variantNM_020796.5(SEMA6A):c.1466G>A (p.Gly489Asp)not specified [RCV004113180]uncertain significance5116478116116478116Humanname
156236392CV2239011single nucleotide variantNM_020796.5(SEMA6A):c.2791G>A (p.Ala931Thr)not specified [RCV004109894]uncertain significance5116446915116446915Humanname
156078105CV2248258single nucleotide variantNM_020796.5(SEMA6A):c.2422T>C (p.Ser808Pro)not specified [RCV004119428]uncertain significance5116447284116447284Humanname
156078123CV2248259single nucleotide variantNM_020796.5(SEMA6A):c.2423C>T (p.Ser808Phe)not specified [RCV004119429]uncertain significance5116447283116447283Humanname
156079289CV2248486single nucleotide variantNM_020796.5(SEMA6A):c.1493C>T (p.Ser498Phe)not specified [RCV004119616]uncertain significance5116478089116478089Humanname
155923624CV2248557single nucleotide variantNM_020796.5(SEMA6A):c.2528T>C (p.Leu843Pro)not specified [RCV004121754]uncertain significance5116447178116447178Humanname
156034828CV2252912single nucleotide variantNM_020796.5(SEMA6A):c.2578A>G (p.Ser860Gly)not specified [RCV004120738]uncertain significance5116447128116447128Humanname
156367717CV2266863single nucleotide variantNM_020796.5(SEMA6A):c.2609T>C (p.Leu870Pro)not specified [RCV004131532]uncertain significance5116447097116447097Humanname
156136260CV2284799single nucleotide variantNM_020796.5(SEMA6A):c.1145A>G (p.Asn382Ser)not specified [RCV004142977]uncertain significance5116480227116480227Humanname
156177157CV2296997single nucleotide variantNM_020796.5(SEMA6A):c.2794A>T (p.Thr932Ser)not specified [RCV004150924]uncertain significance5116446912116446912Humanname
156054212CV2320444single nucleotide variantNM_020796.5(SEMA6A):c.1193T>A (p.Met398Lys)not specified [RCV004172086]uncertain significance5116480179116480179Humanname
156059210CV2343689single nucleotide variantNM_020796.5(SEMA6A):c.1816T>C (p.Trp606Arg)not specified [RCV004190714]uncertain significance5116467661116467661Humanname
155986990CV2354837single nucleotide variantNM_020796.5(SEMA6A):c.2914C>T (p.His972Tyr)not specified [RCV004191335]uncertain significance5116446792116446792Humanname
156005551CV2357673single nucleotide variantNM_020796.5(SEMA6A):c.2455C>T (p.Pro819Ser)not specified [RCV004202931]uncertain significance5116447251116447251Humanname
155964965CV2395900single nucleotide variantNM_020796.5(SEMA6A):c.2462C>T (p.Thr821Met)not specified [RCV004237458]uncertain significance5116447244116447244Humanname
329396750CV2459002single nucleotide variantNM_020796.5(SEMA6A):c.2239C>A (p.Gln747Lys)not specified [RCV004272481]uncertain significance5116447467116447467Humanname
401732682CV2691078single nucleotide variantNM_020796.5(SEMA6A):c.1279A>C (p.Thr427Pro)not specified [RCV004301077]uncertain significance5116478690116478690Humanname
401749026CV2692911single nucleotide variantNM_020796.5(SEMA6A):c.2751G>C (p.Lys917Asn)not specified [RCV004306437]uncertain significance5116446955116446955Humanname
401742236CV2697729single nucleotide variantNM_020796.5(SEMA6A):c.1926C>A (p.His642Gln)not specified [RCV004300465]uncertain significance5116447780116447780Humanname
401759087CV2712404single nucleotide variantNM_020796.5(SEMA6A):c.1132T>C (p.Tyr378His)not specified [RCV004313877]uncertain significance5116480240116480240Humanname
401761606CV2713817single nucleotide variantNM_020796.5(SEMA6A):c.1588G>A (p.Asp530Asn)not specified [RCV004315267]uncertain significance5116477907116477907Humanname
401763660CV2714634single nucleotide variantNM_020796.5(SEMA6A):c.1115C>T (p.Ser372Leu)not specified [RCV004319916]uncertain significance5116480257116480257Humanname
401766005CV2717972single nucleotide variantNM_020796.5(SEMA6A):c.2086C>T (p.Arg696Trp)not specified [RCV004321921]uncertain significance5116447620116447620Humanname
401762560CV2719975single nucleotide variantNM_020796.5(SEMA6A):c.2773C>T (p.Leu925Phe)not specified [RCV004323560]uncertain significance5116446933116446933Humanname
401729738CV2736539single nucleotide variantNM_020796.5(SEMA6A):c.1268T>C (p.Ile423Thr)Delayed puberty, self-limited [RCV003312987]likely pathogenic5116478701116478701Human1name
401883314CV2760956single nucleotide variantNM_020796.5(SEMA6A):c.1853C>A (p.Pro618His)not specified [RCV004336588]uncertain significance5116467624116467624Humanname
401884029CV2764995single nucleotide variantNM_020796.5(SEMA6A):c.2302C>T (p.Arg768Trp)not specified [RCV004337119]uncertain significance5116447404116447404Humanname
405728606CV3317455single nucleotide variantNM_020796.5(SEMA6A):c.1436A>G (p.Tyr479Cys)not specified [RCV004450717]uncertain significance5116478146116478146Humanname
405728621CV3317456single nucleotide variantNM_020796.5(SEMA6A):c.1550G>A (p.Arg517Gln)not specified [RCV004450718]uncertain significance5116478032116478032Humanname
405728630CV3317457single nucleotide variantNM_020796.5(SEMA6A):c.1897G>C (p.Val633Leu)not specified [RCV004450719]uncertain significance5116447809116447809Humanname
405728640CV3317458single nucleotide variantNM_020796.5(SEMA6A):c.2030G>A (p.Arg677Gln)not specified [RCV004450720]uncertain significance5116447676116447676Humanname
405728647CV3317459single nucleotide variantNM_020796.5(SEMA6A):c.2501A>G (p.Lys834Arg)not specified [RCV004450721]uncertain significance5116447205116447205Humanname
405728650CV3317460single nucleotide variantNM_020796.5(SEMA6A):c.2564T>G (p.Ile855Ser)not specified [RCV004450722]uncertain significance5116447142116447142Humanname
405728660CV3317461single nucleotide variantNM_020796.5(SEMA6A):c.2672C>A (p.Pro891Gln)not specified [RCV004450723]uncertain significance5116447034116447034Humanname
405728669CV3317462single nucleotide variantNM_020796.5(SEMA6A):c.2678C>A (p.Ala893Asp)not specified [RCV004450724]uncertain significance5116447028116447028Humanname
405728681CV3317463single nucleotide variantNM_020796.5(SEMA6A):c.2707C>T (p.Arg903Trp)not specified [RCV004450725]uncertain significance5116446999116446999Humanname
407478157CV3473470single nucleotide variantNM_020796.5(SEMA6A):c.2377C>G (p.Pro793Ala)not specified [RCV004663844]uncertain significance5116447329116447329Humanname
407478161CV3473471single nucleotide variantNM_020796.5(SEMA6A):c.2434A>G (p.Ile812Val)not specified [RCV004663845]uncertain significance5116447272116447272Humanname
407478167CV3473472single nucleotide variantNM_020796.5(SEMA6A):c.2872A>C (p.Asn958His)not specified [RCV004663846]uncertain significance5116446834116446834Humanname
407492328CV3473473single nucleotide variantNM_020796.5(SEMA6A):c.2301G>T (p.Lys767Asn)not specified [RCV004667090]uncertain significance5116447405116447405Humanname
407478171CV3473474single nucleotide variantNM_020796.5(SEMA6A):c.2317G>A (p.Gly773Ser)not specified [RCV004663847]uncertain significance5116447389116447389Humanname
407478177CV3473475single nucleotide variantNM_020796.5(SEMA6A):c.1463T>C (p.Met488Thr)not specified [RCV004663848]uncertain significance5116478119116478119Humanname
597736615CV3602047single nucleotide variantNM_020796.5(SEMA6A):c.2041G>A (p.Val681Met)not specified [RCV004863876]uncertain significance5116447665116447665Humanname
597736628CV3602049single nucleotide variantNM_020796.5(SEMA6A):c.1855T>G (p.Leu619Val)not specified [RCV004863878]uncertain significance5116467622116467622Humanname
597736633CV3602050single nucleotide variantNM_020796.5(SEMA6A):c.2057G>A (p.Arg686His)not specified [RCV004863879]uncertain significance5116447649116447649Humanname
597736638CV3602051single nucleotide variantNM_020796.5(SEMA6A):c.2443G>A (p.Val815Met)not specified [RCV004863880]uncertain significance5116447263116447263Humanname
597736648CV3602054single nucleotide variantNM_020796.5(SEMA6A):c.2511G>T (p.Glu837Asp)not specified [RCV004863882]uncertain significance5116447195116447195Humanname
597736652CV3602055single nucleotide variantNM_020796.5(SEMA6A):c.2632C>A (p.Pro878Thr)not specified [RCV004863883]uncertain significance5116447074116447074Humanname
597736661CV3602056single nucleotide variantNM_020796.5(SEMA6A):c.2087G>A (p.Arg696Gln)not specified [RCV004863884]uncertain significance5116447619116447619Humanname
597736665CV3602057single nucleotide variantNM_020796.5(SEMA6A):c.2995G>A (p.Gly999Arg)not specified [RCV004863885]uncertain significance5116446711116446711Humanname
597736675CV3602059single nucleotide variantNM_020796.5(SEMA6A):c.1916T>C (p.Leu639Pro)not specified [RCV004863887]uncertain significance5116447790116447790Humanname
597736695CV3602063single nucleotide variantNM_020796.5(SEMA6A):c.1399G>A (p.Glu467Lys)not specified [RCV004863891]uncertain significance5116478570116478570Humanname
597736706CV3602066single nucleotide variantNM_020796.5(SEMA6A):c.1477G>C (p.Asp493His)not specified [RCV004863893]uncertain significance5116478105116478105Humanname
597736717CV3602068single nucleotide variantNM_020796.5(SEMA6A):c.2288C>G (p.Thr763Arg)not specified [RCV004863895]uncertain significance5116447418116447418Humanname
597736722CV3602069single nucleotide variantNM_020796.5(SEMA6A):c.1305C>A (p.His435Gln)not specified [RCV004863896]uncertain significance5116478664116478664Humanname
597736732CV3602071single nucleotide variantNM_020796.5(SEMA6A):c.1428A>C (p.Lys476Asn)not specified [RCV004863898]uncertain significance5116478154116478154Humanname
598224044CV3904063single nucleotide variantNM_020796.5(SEMA6A):c.2986A>T (p.Thr996Ser)not specified [RCV005273140]uncertain significance5116446720116446720Humanname
598224068CV3904067single nucleotide variantNM_020796.5(SEMA6A):c.2838C>A (p.His946Gln)not specified [RCV005273144]uncertain significance5116446868116446868Humanname
598224076CV3904068single nucleotide variantNM_020796.5(SEMA6A):c.2002A>G (p.Ile668Val)not specified [RCV005273145]uncertain significance5116447704116447704Humanname
598224083CV3904069single nucleotide variantNM_020796.5(SEMA6A):c.2290C>G (p.Leu764Val)not specified [RCV005273146]uncertain significance5116447416116447416Humanname
598224090CV3904070single nucleotide variantNM_020796.5(SEMA6A):c.2203C>A (p.Pro735Thr)not specified [RCV005273147]uncertain significance5116447503116447503Humanname
598224106CV3904072single nucleotide variantNM_020796.5(SEMA6A):c.1217T>A (p.Phe406Tyr)not specified [RCV005273149]uncertain significance5116480155116480155Humanname
15200944CV721163single nucleotide variantNM_020796.5(SEMA6A):c.2909A>C (p.Gln970Pro)not provided [RCV000891053]benign|likely benign5116446797116446797Humanname
15176073CV721164single nucleotide variantNM_020796.5(SEMA6A):c.2791G>C (p.Ala931Pro)not provided [RCV000884505]likely benign5116446915116446915Humanname
15181953CV721165single nucleotide variantNM_020796.5(SEMA6A):c.2672C>T (p.Pro891Leu)not provided [RCV000885881]likely benign5116447034116447034Humanname
15124417CV734808single nucleotide variantNM_020796.5(SEMA6A):c.1613A>G (p.Glu538Gly)not provided [RCV000896584]likely benign5116477882116477882Humanname
156068013CV2237015single nucleotide variantNM_020796.5(SEMA6A):c.3028G>A (p.Val1010Ile)not specified [RCV004113000]uncertain significance5116446678116446678Humanname
156197519CV2293576single nucleotide variantNM_020796.5(SEMA6A):c.2998C>G (p.Leu1000Val)not specified [RCV004153100]uncertain significance5116446708116446708Humanname
155935145CV2371736single nucleotide variantNM_020796.5(SEMA6A):c.3008C>T (p.Thr1003Met)not specified [RCV004219404]uncertain significance5116446698116446698Humanname
401763873CV2725340single nucleotide variantNM_020796.5(SEMA6A):c.3017T>G (p.Leu1006Arg)not specified [RCV004319996]uncertain significance5116446689116446689Humanname