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Variants search result for Homo sapiens
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51 records found for search term Mavs
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15201662CV731345single nucleotide variantNM_020746.5(MAVS):c.292+3G>Anot provided [RCV000891255]benign2038578123857812Humanname
15114432CV780210single nucleotide variantNM_020746.5(MAVS):c.292+6C>Tnot provided [RCV000961674]benign2038578153857815Humanname
15128426CV716971single nucleotide variantNM_020746.5(MAVS):c.198C>T (p.Pro66=)not provided [RCV000964082]benign2038577153857715Humanname
155966183CV2216616single nucleotide variantNM_020746.5(MAVS):c.41G>A (p.Arg14His)not specified [RCV004081026]likely benign2038546653854665Humanname
156072795CV2233397single nucleotide variantNM_020746.5(MAVS):c.40C>T (p.Arg14Cys)not specified [RCV004105757]uncertain significance2038546643854664Humanname
597637653CV3694403single nucleotide variantNM_020746.5(MAVS):c.34A>G (p.Ile12Val)not specified [RCV004941012]uncertain significance2038546583854658Humanname
155925232CV2211775single nucleotide variantNM_020746.5(MAVS):c.253G>A (p.Ala85Thr)not specified [RCV004086614]uncertain significance2038577703857770Humanname
156157545CV2235305single nucleotide variantNM_020746.5(MAVS):c.254C>T (p.Ala85Val)not specified [RCV004107339]uncertain significance2038577713857771Humanname
156154937CV2374972single nucleotide variantNM_020746.5(MAVS):c.290C>T (p.Pro97Leu)not specified [RCV004227987]uncertain significance2038578073857807Humanname
401919617CV2827086single nucleotide variantNM_020746.5(MAVS):c.1266C>T (p.Gly422=)not provided [RCV003431252]likely benign2038657903865790Humanname
405659518CV3278133single nucleotide variantNM_020746.5(MAVS):c.278A>G (p.Gln93Arg)not specified [RCV004416808]uncertain significance2038577953857795Humanname
407469364CV3457035single nucleotide variantNM_020746.5(MAVS):c.128G>C (p.Arg43Pro)not specified [RCV004636598]uncertain significance2038576453857645Humanname
597637659CV3694404single nucleotide variantNM_020746.5(MAVS):c.221C>T (p.Ala74Val)not specified [RCV004941013]uncertain significance2038577383857738Humanname
15177935CV705480single nucleotide variantNM_020746.5(MAVS):c.1491C>T (p.Ala497=)not provided [RCV000951156]benign2038660153866015Humanname
15128429CV716972single nucleotide variantNM_020746.5(MAVS):c.1473C>T (p.Gly491=)not provided [RCV000964083]likely benign2038659973865997Humanname
15140726CV742399single nucleotide variantNM_020746.5(MAVS):c.1077G>A (p.Val359=)not provided [RCV000899368]likely benign2038647073864707Humanname
155931056CV2297208single nucleotide variantNM_020746.5(MAVS):c.305G>A (p.Arg102His)not specified [RCV004151095]uncertain significance2038613443861344Humanname
156269713CV2315035single nucleotide variantNM_020746.5(MAVS):c.892G>A (p.Val298Met)not specified [RCV004164947]uncertain significance2038645223864522Humanname
155962496CV2388247single nucleotide variantNM_020746.5(MAVS):c.689T>C (p.Leu230Pro)not specified [RCV004234705]uncertain significance2038643193864319Humanname
156163528CV2389589single nucleotide variantNM_020746.5(MAVS):c.653G>A (p.Arg218His)not specified [RCV004243654]uncertain significance2038642833864283Humanname
329394924CV2457733single nucleotide variantNM_020746.5(MAVS):c.749C>T (p.Thr250Ile)not specified [RCV004269572]uncertain significance2038643793864379Humanname
401749596CV2694681single nucleotide variantNM_020746.5(MAVS):c.596A>G (p.Asp199Gly)not specified [RCV004298784]uncertain significance2038623843862384Humanname
401897852CV2773016single nucleotide variantNM_020746.5(MAVS):c.421C>G (p.Pro141Ala)not specified [RCV004351466]uncertain significance2038614603861460Humanname
405659524CV3278135single nucleotide variantNM_020746.5(MAVS):c.773C>T (p.Ser258Phe)not specified [RCV004416810]uncertain significance2038644033864403Humanname
407469367CV3457036single nucleotide variantNM_020746.5(MAVS):c.589G>A (p.Glu197Lys)not specified [RCV004636599]uncertain significance2038623773862377Humanname
597637647CV3694401single nucleotide variantNM_020746.5(MAVS):c.908T>C (p.Met303Thr)not specified [RCV004941011]uncertain significance2038645383864538Humanname
597637664CV3694405single nucleotide variantNM_020746.5(MAVS):c.581G>C (p.Gly194Ala)not specified [RCV004941014]uncertain significance2038623693862369Humanname
598199549CV3981744single nucleotide variantNM_020746.5(MAVS):c.962C>T (p.Thr321Ile)not specified [RCV005375714]uncertain significance2038645923864592Humanname
598177495CV3981745single nucleotide variantNM_020746.5(MAVS):c.356C>T (p.Pro119Leu)not specified [RCV005371606]uncertain significance2038613953861395Humanname
156242621CV2246250single nucleotide variantNM_020746.5(MAVS):c.1298C>T (p.Ser433Leu)not specified [RCV004107706]uncertain significance2038658223865822Humanname
155995544CV2259097single nucleotide variantNM_020746.5(MAVS):c.1301G>T (p.Gly434Val)not specified [RCV004120352]uncertain significance2038658253865825Humanname
156146929CV2265167single nucleotide variantNM_020746.5(MAVS):c.1352C>T (p.Pro451Leu)not specified [RCV004126293]uncertain significance2038658763865876Humanname
155972892CV2271586single nucleotide variantNM_020746.5(MAVS):c.1067C>G (p.Ala356Gly)not specified [RCV004128667]uncertain significance2038646973864697Humanname
155992661CV2379336single nucleotide variantNM_020746.5(MAVS):c.1606C>T (p.Arg536Trp)not specified [RCV004223797]uncertain significance2038661303866130Humanname
156158595CV2398048single nucleotide variantNM_020746.5(MAVS):c.1582G>C (p.Val528Leu)not specified [RCV004241638]uncertain significance2038661063866106Humanname
401749402CV2702766single nucleotide variantNM_020746.5(MAVS):c.1557G>C (p.Gln519His)not specified [RCV004319336]uncertain significance2038660813866081Humanname
401757968CV2731588single nucleotide variantNM_020746.5(MAVS):c.1267G>A (p.Val423Met)not specified [RCV004330933]likely benign2038657913865791Humanname
401860365CV2762410single nucleotide variantNM_020746.5(MAVS):c.1597G>A (p.Val533Met)not specified [RCV004335515]uncertain significance2038661213866121Humanname
401885220CV2770977single nucleotide variantNM_020746.5(MAVS):c.1428C>G (p.Ile476Met)not specified [RCV004343997]uncertain significance2038659523865952Humanname
401892269CV2777379single nucleotide variantNM_020746.5(MAVS):c.1568C>T (p.Thr523Ile)not specified [RCV004354384]uncertain significance2038660923866092Humanname
405659500CV3278127single nucleotide variantNM_020746.5(MAVS):c.1022T>C (p.Leu341Pro)not specified [RCV004416802]uncertain significance2038646523864652Humanname
405659502CV3278128single nucleotide variantNM_020746.5(MAVS):c.1292C>T (p.Pro431Leu)not specified [RCV004416803]uncertain significance2038658163865816Humanname
405659505CV3278129single nucleotide variantNM_020746.5(MAVS):c.1304G>C (p.Cys435Ser)not specified [RCV004416804]uncertain significance2038658283865828Humanname
405659508CV3278130single nucleotide variantNM_020746.5(MAVS):c.1409T>C (p.Val470Ala)not specified [RCV004416805]uncertain significance2038659333865933Humanname
405659515CV3278132single nucleotide variantNM_020746.5(MAVS):c.1613G>A (p.Arg538His)not specified [RCV004416807]uncertain significance2038661373866137Humanname
407473152CV3457037single nucleotide variantNM_020746.5(MAVS):c.1127C>T (p.Thr376Ile)not specified [RCV004637704]uncertain significance2038647573864757Humanname
597637671CV3694406single nucleotide variantNM_020746.5(MAVS):c.1309G>C (p.Glu437Gln)not specified [RCV004941015]uncertain significance2038658333865833Humanname
598177501CV3981746single nucleotide variantNM_020746.5(MAVS):c.1142G>A (p.Gly381Glu)not specified [RCV005371607]uncertain significance2038647723864772Humanname
598199557CV3981748single nucleotide variantNM_020746.5(MAVS):c.1260G>C (p.Lys420Asn)not specified [RCV005375715]uncertain significance2038657843865784Humanname
13820733CV576187single nucleotide variantNM_020746.5(MAVS):c.1189G>A (p.Ala397Thr)not provided [RCV000709788]not provided2038657133865713Humanname
15163207CV705479single nucleotide variantNM_020746.5(MAVS):c.1237G>A (p.Gly413Ser)not provided [RCV000948029]benign2038657613865761Humanname