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91 records found for search term Chsy3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8580356CV114786single nucleotide variantNM_175856.4(CHSY3):c.1086+77222T>CLung cancer [RCV000095309]uncertain significance5129985582129985582Humanname
597771195CV3650109single nucleotide variantNM_175856.5(CHSY3):c.35T>C (p.Val12Ala)not specified [RCV004897077]uncertain significance5129904864129904864Humanname
156249979CV2273231single nucleotide variantNM_175856.5(CHSY3):c.164C>A (p.Pro55His)not specified [RCV004132027]uncertain significance5129904993129904993Humanname
156173798CV2326883single nucleotide variantNM_175856.5(CHSY3):c.212G>C (p.Arg71Pro)not specified [RCV004176706]uncertain significance5129905041129905041Humanname
155905152CV2349690single nucleotide variantNM_175856.5(CHSY3):c.197C>T (p.Pro66Leu)not specified [RCV004204106]likely benign5129905026129905026Humanname
156138789CV2374250single nucleotide variantNM_175856.5(CHSY3):c.242A>G (p.Gln81Arg)not specified [RCV004229387]uncertain significance5129905071129905071Humanname
156104305CV2386957single nucleotide variantNM_175856.5(CHSY3):c.205C>G (p.Arg69Gly)not specified [RCV004233582]uncertain significance5129905034129905034Humanname
329377900CV2460816single nucleotide variantNM_175856.5(CHSY3):c.280G>A (p.Gly94Arg)not specified [RCV004271134]uncertain significance5129905109129905109Humanname
401879538CV2769646single nucleotide variantNM_175856.5(CHSY3):c.158C>T (p.Ala53Val)not specified [RCV004351575]uncertain significance5129904987129904987Humanname
405672859CV3293584single nucleotide variantNM_175856.5(CHSY3):c.2574C>T (p.Phe858=)not specified [RCV004441660]likely benign5130185716130185716Humanname
407456085CV3422956single nucleotide variantNM_175856.5(CHSY3):c.281G>A (p.Gly94Glu)not specified [RCV004610585]uncertain significance5129905110129905110Humanname
407456090CV3422958single nucleotide variantNM_175856.5(CHSY3):c.179A>T (p.Gln60Leu)not specified [RCV004610587]uncertain significance5129905008129905008Humanname
596945654CV3547981single nucleotide variantNM_175856.5(CHSY3):c.2529C>T (p.Asp843=)not provided [RCV004809312]likely benign5130185671130185671Humanname
597771173CV3650103single nucleotide variantNM_175856.5(CHSY3):c.145G>C (p.Gly49Arg)not specified [RCV004897072]uncertain significance5129904974129904974Humanname
598230037CV3951883single nucleotide variantNM_175856.5(CHSY3):c.166C>A (p.Arg56Ser)not specified [RCV005319332]uncertain significance5129904995129904995Humanname
156213750CV2257399single nucleotide variantNM_175856.5(CHSY3):c.511G>C (p.Asp171His)not specified [RCV004125486]uncertain significance5129905340129905340Humanname
156334133CV2267052single nucleotide variantNM_175856.5(CHSY3):c.768G>T (p.Trp256Cys)not specified [RCV004131688]uncertain significance5129905597129905597Humanname
155973492CV2332406single nucleotide variantNM_175856.5(CHSY3):c.479G>A (p.Gly160Glu)not specified [RCV004196137]uncertain significance5129905308129905308Humanname
156081859CV2333393single nucleotide variantNM_175856.5(CHSY3):c.752T>C (p.Leu251Pro)not specified [RCV004190100]uncertain significance5129905581129905581Humanname
155994610CV2377570single nucleotide variantNM_175856.5(CHSY3):c.590G>A (p.Arg197His)not specified [RCV004227765]uncertain significance5129905419129905419Humanname
156388185CV2380176single nucleotide variantNM_175856.5(CHSY3):c.421G>A (p.Ala141Thr)not specified [RCV004224544]uncertain significance5129905250129905250Humanname
156048821CV2391039single nucleotide variantNM_175856.5(CHSY3):c.466G>C (p.Gly156Arg)not specified [RCV004235035]uncertain significance5129905295129905295Humanname
155996519CV2393193single nucleotide variantNM_175856.5(CHSY3):c.479G>C (p.Gly160Ala)not specified [RCV004226668]uncertain significance5129905308129905308Humanname
156160768CV2398218single nucleotide variantNM_175856.5(CHSY3):c.433C>T (p.Arg145Trp)not specified [RCV004235134]uncertain significance5129905262129905262Humanname
156165520CV2398829single nucleotide variantNM_175856.5(CHSY3):c.985A>G (p.Ile329Val)not specified [RCV004245152]uncertain significance5129908259129908259Humanname
329374042CV2434677single nucleotide variantNM_175856.5(CHSY3):c.989G>T (p.Gly330Val)not specified [RCV004248395]uncertain significance5129908263129908263Humanname
405672864CV3293585single nucleotide variantNM_175856.5(CHSY3):c.437G>C (p.Arg146Thr)not specified [RCV004441661]uncertain significance5129905266129905266Humanname
405672868CV3293586single nucleotide variantNM_175856.5(CHSY3):c.650C>G (p.Pro217Arg)not specified [RCV004441662]uncertain significance5129905479129905479Humanname
405672872CV3293587single nucleotide variantNM_175856.5(CHSY3):c.674C>G (p.Ala225Gly)not specified [RCV004441663]uncertain significance5129905503129905503Humanname
405672874CV3293588single nucleotide variantNM_175856.5(CHSY3):c.854A>T (p.Tyr285Phe)not specified [RCV004441664]uncertain significance5129908128129908128Humanname
597771191CV3650108single nucleotide variantNM_175856.5(CHSY3):c.465C>A (p.Asn155Lys)not specified [RCV004897076]uncertain significance5129905294129905294Humanname
597771210CV3650112single nucleotide variantNM_175856.5(CHSY3):c.698A>G (p.Tyr233Cys)not specified [RCV004897080]uncertain significance5129905527129905527Humanname
598230043CV3951885single nucleotide variantNM_175856.5(CHSY3):c.335G>A (p.Arg112Gln)not specified [RCV005319333]uncertain significance5129905164129905164Humanname
598230064CV3951888single nucleotide variantNM_175856.5(CHSY3):c.639C>G (p.Asn213Lys)not specified [RCV005319336]uncertain significance5129905468129905468Humanname
156068230CV2193708single nucleotide variantNM_175856.5(CHSY3):c.1000A>G (p.Arg334Gly)not specified [RCV004074302]uncertain significance5129908274129908274Humanname
156372651CV2194503single nucleotide variantNM_175856.5(CHSY3):c.2027G>A (p.Gly676Glu)not specified [RCV004081574]likely benign5130185169130185169Humanname
156017899CV2223013single nucleotide variantNM_175856.5(CHSY3):c.1045G>A (p.Val349Ile)not specified [RCV004103600]uncertain significance5129908319129908319Humanname
156386070CV2228108single nucleotide variantNM_175856.5(CHSY3):c.1171A>G (p.Ile391Val)not specified [RCV004096333]uncertain significance5130184313130184313Humanname
156282379CV2252401single nucleotide variantNM_175856.5(CHSY3):c.2377G>A (p.Ala793Thr)not specified [RCV004116242]uncertain significance5130185519130185519Humanname
156310843CV2260100single nucleotide variantNM_175856.5(CHSY3):c.1760T>A (p.Ile587Asn)not specified [RCV004119103]uncertain significance5130184902130184902Humanname
156244517CV2267380single nucleotide variantNM_175856.5(CHSY3):c.2306C>T (p.Ser769Leu)not specified [RCV004134036]uncertain significance5130185448130185448Humanname
156287146CV2288370single nucleotide variantNM_175856.5(CHSY3):c.1724C>T (p.Thr575Ile)not specified [RCV004151927]uncertain significance5130184866130184866Humanname
156057400CV2305129single nucleotide variantNM_175856.5(CHSY3):c.1093C>A (p.Gln365Lys)not specified [RCV004171078]uncertain significance5130184235130184235Humanname
156207440CV2307945single nucleotide variantNM_175856.5(CHSY3):c.2473C>G (p.Gln825Glu)not specified [RCV004170388]uncertain significance5130185615130185615Humanname
156074889CV2321726single nucleotide variantNM_175856.5(CHSY3):c.1847A>C (p.His616Pro)not specified [RCV004179722]uncertain significance5130184989130184989Humanname
156291251CV2324983single nucleotide variantNM_175856.5(CHSY3):c.1873G>C (p.Val625Leu)not specified [RCV004175231]uncertain significance5130185015130185015Humanname
156187943CV2328494single nucleotide variantNM_175856.5(CHSY3):c.1490A>G (p.Asp497Gly)not specified [RCV004175871]uncertain significance5130184632130184632Humanname
156047372CV2336365single nucleotide variantNM_175856.5(CHSY3):c.2396C>T (p.Ser799Leu)not specified [RCV004194586]uncertain significance5130185538130185538Humanname
155920490CV2350515single nucleotide variantNM_175856.5(CHSY3):c.1386A>C (p.Glu462Asp)not specified [RCV004204876]uncertain significance5130184528130184528Humanname
156190594CV2356760single nucleotide variantNM_175856.5(CHSY3):c.1495G>A (p.Val499Ile)not specified [RCV004202105]uncertain significance5130184637130184637Humanname
156128165CV2358382single nucleotide variantNM_175856.5(CHSY3):c.2405G>T (p.Gly802Val)not specified [RCV004207277]uncertain significance5130185547130185547Humanname
156213622CV2367108single nucleotide variantNM_175856.5(CHSY3):c.1932G>T (p.Met644Ile)not specified [RCV004215551]uncertain significance5130185074130185074Humanname
156053915CV2388570single nucleotide variantNM_175856.5(CHSY3):c.1737T>G (p.Asp579Glu)not specified [RCV004237416]uncertain significance5130184879130184879Humanname
329353985CV2436729single nucleotide variantNM_175856.5(CHSY3):c.1933T>C (p.Cys645Arg)not specified [RCV004258097]uncertain significance5130185075130185075Humanname
329371983CV2454952single nucleotide variantNM_175856.5(CHSY3):c.1121A>G (p.Asn374Ser)not specified [RCV004272232]uncertain significance5130184263130184263Humanname
329359924CV2462223single nucleotide variantNM_175856.5(CHSY3):c.1624C>T (p.Leu542Phe)not specified [RCV004266227]uncertain significance5130184766130184766Humanname
401726196CV2695600single nucleotide variantNM_175856.5(CHSY3):c.2575G>A (p.Ala859Thr)not specified [RCV004299420]uncertain significance5130185717130185717Humanname
401760897CV2706138single nucleotide variantNM_175856.5(CHSY3):c.1879C>G (p.Leu627Val)not specified [RCV004314823]uncertain significance5130185021130185021Humanname
401770306CV2711066single nucleotide variantNM_175856.5(CHSY3):c.2188C>G (p.Arg730Gly)not specified [RCV004310758]uncertain significance5130185330130185330Humanname
401761480CV2726785single nucleotide variantNM_175856.5(CHSY3):c.1458C>A (p.Ser486Arg)not specified [RCV004323098]uncertain significance5130184600130184600Humanname
401761913CV2726958single nucleotide variantNM_175856.5(CHSY3):c.1322A>C (p.Lys441Thr)not specified [RCV004325028]uncertain significance5130184464130184464Humanname
401897668CV2772732single nucleotide variantNM_175856.5(CHSY3):c.2204C>A (p.Thr735Lys)not specified [RCV004357540]uncertain significance5130185346130185346Humanname
401873632CV2776643single nucleotide variantNM_175856.5(CHSY3):c.1990G>A (p.Gly664Ser)not specified [RCV004357512]uncertain significance5130185132130185132Humanname
401886683CV2776691single nucleotide variantNM_175856.5(CHSY3):c.2090G>T (p.Arg697Ile)not specified [RCV004357854]uncertain significance5130185232130185232Humanname
401876233CV2777717single nucleotide variantNM_175856.5(CHSY3):c.2566A>C (p.Ser856Arg)not specified [RCV004345553]uncertain significance5130185708130185708Humanname
401865046CV2791460single nucleotide variantNM_175856.5(CHSY3):c.1561G>A (p.Glu521Lys)not specified [RCV004358849]uncertain significance5130184703130184703Humanname
405672818CV3293574single nucleotide variantNM_175856.5(CHSY3):c.1124G>A (p.Arg375Gln)not specified [RCV004441650]uncertain significance5130184266130184266Humanname
405672827CV3293576single nucleotide variantNM_175856.5(CHSY3):c.1467C>G (p.Ser489Arg)not specified [RCV004441652]uncertain significance5130184609130184609Humanname
405672831CV3293577single nucleotide variantNM_175856.5(CHSY3):c.1507A>G (p.Met503Val)not specified [RCV004441653]uncertain significance5130184649130184649Humanname
405672835CV3293578single nucleotide variantNM_175856.5(CHSY3):c.1519A>G (p.Asn507Asp)not specified [RCV004441654]uncertain significance5130184661130184661Humanname
405672839CV3293579single nucleotide variantNM_175856.5(CHSY3):c.1580G>T (p.Arg527Leu)not specified [RCV004441655]uncertain significance5130184722130184722Humanname
405672844CV3293580single nucleotide variantNM_175856.5(CHSY3):c.1885G>A (p.Gly629Arg)not specified [RCV004441656]uncertain significance5130185027130185027Humanname
405672853CV3293582single nucleotide variantNM_175856.5(CHSY3):c.2065A>C (p.Ile689Leu)not specified [RCV004441658]uncertain significance5130185207130185207Humanname
405672857CV3293583single nucleotide variantNM_175856.5(CHSY3):c.2431T>C (p.Tyr811His)not specified [RCV004441659]uncertain significance5130185573130185573Humanname
407456087CV3422957single nucleotide variantNM_175856.5(CHSY3):c.2393C>T (p.Thr798Ile)not specified [RCV004610586]uncertain significance5130185535130185535Humanname
407456092CV3422959single nucleotide variantNM_175856.5(CHSY3):c.1544G>A (p.Arg515Gln)not specified [RCV004610588]uncertain significance5130184686130184686Humanname
407456095CV3422960single nucleotide variantNM_175856.5(CHSY3):c.1890G>T (p.Arg630Ser)not specified [RCV004610589]uncertain significance5130185032130185032Humanname
407456098CV3422961single nucleotide variantNM_175856.5(CHSY3):c.1972C>A (p.Leu658Ile)not specified [RCV004610590]uncertain significance5130185114130185114Humanname
407456100CV3422962single nucleotide variantNM_175856.5(CHSY3):c.1814C>A (p.Ser605Tyr)not specified [RCV004610591]uncertain significance5130184956130184956Humanname
597771178CV3650104single nucleotide variantNM_175856.5(CHSY3):c.1439A>G (p.Asn480Ser)not specified [RCV004897073]uncertain significance5130184581130184581Humanname
597771183CV3650106single nucleotide variantNM_175856.5(CHSY3):c.2284A>G (p.Thr762Ala)not specified [RCV004897074]uncertain significance5130185426130185426Humanname
597771186CV3650107single nucleotide variantNM_175856.5(CHSY3):c.2269G>A (p.Gly757Arg)not specified [RCV004897075]uncertain significance5130185411130185411Humanname
597771200CV3650110single nucleotide variantNM_175856.5(CHSY3):c.1923T>G (p.Phe641Leu)not specified [RCV004897078]uncertain significance5130185065130185065Humanname
597771205CV3650111single nucleotide variantNM_175856.5(CHSY3):c.2567G>C (p.Ser856Thr)not specified [RCV004897079]uncertain significance5130185709130185709Humanname
597771212CV3650113single nucleotide variantNM_175856.5(CHSY3):c.1342G>C (p.Val448Leu)not specified [RCV004897081]uncertain significance5130184484130184484Humanname
597771217CV3650114single nucleotide variantNM_175856.5(CHSY3):c.2053G>A (p.Glu685Lys)not specified [RCV004897082]uncertain significance5130185195130185195Humanname
598230014CV3951879single nucleotide variantNM_175856.5(CHSY3):c.1742A>G (p.Asn581Ser)not specified [RCV005319328]uncertain significance5130184884130184884Humanname
598230020CV3951880single nucleotide variantNM_175856.5(CHSY3):c.2114C>T (p.Ser705Phe)not specified [RCV005319329]uncertain significance5130185256130185256Humanname
598264447CV3951884single nucleotide variantNM_175856.5(CHSY3):c.1936C>T (p.Leu646Phe)not specified [RCV005326133]uncertain significance5130185078130185078Humanname
598230049CV3951886single nucleotide variantNM_175856.5(CHSY3):c.1183C>T (p.Pro395Ser)not specified [RCV005319334]uncertain significance5130184325130184325Humanname
598230057CV3951887single nucleotide variantNM_175856.5(CHSY3):c.2546T>C (p.Met849Thr)not specified [RCV005319335]uncertain significance5130185688130185688Humanname