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Variants search result for Homo sapiens
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64 records found for search term Zw10
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401759420CV2708659single nucleotide variantNM_004724.4(ZW10):c.33C>G (p.His11Gln)not specified [RCV004307642]uncertain significance11113773634113773634Humanname
407499745CV3421142single nucleotide variantNM_004724.4(ZW10):c.68G>A (p.Arg23Gln)not specified [RCV004606950]uncertain significance11113773599113773599Humanname
401876840CV2754515single nucleotide variantNM_004724.4(ZW10):c.167C>T (p.Ala56Val)not specified [RCV004336721]uncertain significance11113768906113768906Humanname
405689461CV3351509single nucleotide variantNM_004724.4(ZW10):c.268G>A (p.Gly90Ser)not specified [RCV004490459]uncertain significance11113760891113760891Humanname
597758559CV3646450single nucleotide variantNM_004724.4(ZW10):c.208A>G (p.Ile70Val)not specified [RCV004894343]uncertain significance11113768865113768865Humanname
598276504CV3938446single nucleotide variantNM_004724.4(ZW10):c.230T>C (p.Ile77Thr)not specified [RCV005305638]uncertain significance11113768843113768843Humanname
156326123CV2205590single nucleotide variantNM_004724.4(ZW10):c.845C>T (p.Thr282Ile)not specified [RCV004082513]uncertain significance11113757742113757742Humanname
156383086CV2223766single nucleotide variantNM_004724.4(ZW10):c.409C>T (p.Arg137Cys)not specified [RCV004093843]uncertain significance11113760524113760524Humanname
155971313CV2237408single nucleotide variantNM_004724.4(ZW10):c.827G>A (p.Arg276His)not specified [RCV004106378]uncertain significance11113757760113757760Humanname
155955202CV2274429single nucleotide variantNM_004724.4(ZW10):c.743T>G (p.Leu248Arg)not specified [RCV004136799]uncertain significance11113757844113757844Humanname
155920062CV2279533single nucleotide variantNM_004724.4(ZW10):c.698T>C (p.Val233Ala)not specified [RCV004142048]uncertain significance11113758589113758589Humanname
155921699CV2340498single nucleotide variantNM_004724.4(ZW10):c.946C>A (p.Leu316Met)not specified [RCV004197221]uncertain significance11113748400113748400Humanname
156056184CV2371022single nucleotide variantNM_004724.4(ZW10):c.605T>C (p.Leu202Pro)not specified [RCV004220789]uncertain significance11113758682113758682Humanname
401735926CV2672778single nucleotide variantNM_004724.4(ZW10):c.410G>A (p.Arg137His)not specified [RCV004281562]likely benign11113760523113760523Humanname
405689468CV3351511single nucleotide variantNM_004724.4(ZW10):c.362A>G (p.Glu121Gly)not specified [RCV004490461]uncertain significance11113760571113760571Humanname
405689473CV3351512single nucleotide variantNM_004724.4(ZW10):c.451A>G (p.Arg151Gly)not specified [RCV004490462]uncertain significance11113760338113760338Humanname
405689478CV3351513single nucleotide variantNM_004724.4(ZW10):c.463G>T (p.Asp155Tyr)not specified [RCV004490463]uncertain significance11113760326113760326Humanname
405689484CV3351514single nucleotide variantNM_004724.4(ZW10):c.613G>A (p.Glu205Lys)not specified [RCV004490464]uncertain significance11113758674113758674Humanname
405689488CV3351515single nucleotide variantNM_004724.4(ZW10):c.661A>G (p.Met221Val)not specified [RCV004490465]likely benign11113758626113758626Humanname
405689493CV3351516single nucleotide variantNM_004724.4(ZW10):c.674G>T (p.Ser225Ile)not specified [RCV004490466]uncertain significance11113758613113758613Humanname
407493751CV3421146single nucleotide variantNM_004724.4(ZW10):c.682C>T (p.Leu228Phe)not specified [RCV004605424]uncertain significance11113758605113758605Humanname
407499751CV3421151single nucleotide variantNM_004724.4(ZW10):c.833A>C (p.Glu278Ala)not specified [RCV004606952]uncertain significance11113757754113757754Humanname
407493771CV3421153single nucleotide variantNM_004724.4(ZW10):c.499A>G (p.Thr167Ala)not specified [RCV004605429]uncertain significance11113760290113760290Humanname
597758621CV3642586single nucleotide variantNM_004724.4(ZW10):c.979G>A (p.Ala327Thr)not specified [RCV004894355]uncertain significance11113748367113748367Humanname
597758548CV3646448single nucleotide variantNM_004724.4(ZW10):c.803G>A (p.Ser268Asn)not specified [RCV004894341]likely benign11113757784113757784Humanname
597758575CV3646453single nucleotide variantNM_004724.4(ZW10):c.764C>T (p.Pro255Leu)not specified [RCV004894346]uncertain significance11113757823113757823Humanname
597758616CV3646461single nucleotide variantNM_004724.4(ZW10):c.799G>A (p.Glu267Lys)not specified [RCV004894354]uncertain significance11113757788113757788Humanname
598276508CV3938450single nucleotide variantNM_004724.4(ZW10):c.661A>C (p.Met221Leu)not specified [RCV005305642]uncertain significance11113758626113758626Humanname
598201192CV3938451single nucleotide variantNM_004724.4(ZW10):c.553A>C (p.Ile185Leu)not specified [RCV005314186]uncertain significance11113760236113760236Humanname
156079670CV2226564single nucleotide variantNM_004724.4(ZW10):c.1656G>T (p.Leu552Phe)not specified [RCV004101820]uncertain significance11113739310113739310Humanname
155985403CV2247863single nucleotide variantNM_004724.4(ZW10):c.1807A>G (p.Arg603Gly)not specified [RCV004121320]uncertain significance11113738341113738341Humanname
155994797CV2278014single nucleotide variantNM_004724.4(ZW10):c.2307A>C (p.Glu769Asp)not specified [RCV004141246]uncertain significance11113733727113733727Humanname
156269352CV2293245single nucleotide variantNM_004724.4(ZW10):c.1433G>A (p.Arg478His)not specified [RCV004150748]uncertain significance11113743880113743880Humanname
156292442CV2321211single nucleotide variantNM_004724.4(ZW10):c.2102C>T (p.Ser701Phe)not specified [RCV004175331]uncertain significance11113736737113736737Humanname
156133895CV2346900single nucleotide variantNM_004724.4(ZW10):c.2285G>A (p.Arg762His)not specified [RCV004202358]uncertain significance11113733749113733749Humanname
156255830CV2359488single nucleotide variantNM_004724.4(ZW10):c.1468G>A (p.Ala490Thr)not specified [RCV004214800]uncertain significance11113743845113743845Humanname
156105938CV2361359single nucleotide variantNM_004724.4(ZW10):c.1324G>T (p.Asp442Tyr)not specified [RCV004218561]uncertain significance11113743989113743989Humanname
156384163CV2371306single nucleotide variantNM_004724.4(ZW10):c.1634G>C (p.Cys545Ser)not specified [RCV004223318]uncertain significance11113739332113739332Humanname
156392422CV2386312single nucleotide variantNM_004724.4(ZW10):c.2119A>G (p.Lys707Glu)not specified [RCV004228655]uncertain significance11113736720113736720Humanname
401720887CV2702175single nucleotide variantNM_004724.4(ZW10):c.1702T>C (p.Cys568Arg)not specified [RCV004314525]uncertain significance11113739264113739264Humanname
401881071CV2763232single nucleotide variantNM_004724.4(ZW10):c.1319A>G (p.Asp440Gly)not specified [RCV004336266]uncertain significance11113743994113743994Humanname
405689457CV3351508single nucleotide variantNM_004724.4(ZW10):c.1879C>T (p.Arg627Trp)not specified [RCV004490458]uncertain significance11113738269113738269Humanname
407493740CV3421143single nucleotide variantNM_004724.4(ZW10):c.1732G>T (p.Val578Leu)not specified [RCV004605421]uncertain significance11113739234113739234Humanname
407493742CV3421144single nucleotide variantNM_004724.4(ZW10):c.1426A>G (p.Thr476Ala)not specified [RCV004605422]uncertain significance11113743887113743887Humanname
407493747CV3421145single nucleotide variantNM_004724.4(ZW10):c.1219G>A (p.Val407Met)not specified [RCV004605423]uncertain significance11113747584113747584Humanname
407493754CV3421148single nucleotide variantNM_004724.4(ZW10):c.1880G>A (p.Arg627Gln)not specified [RCV004605425]uncertain significance11113738268113738268Humanname
407493757CV3421149single nucleotide variantNM_004724.4(ZW10):c.1177C>T (p.Arg393Cys)not specified [RCV004605426]uncertain significance11113747626113747626Humanname
407493761CV3421150single nucleotide variantNM_004724.4(ZW10):c.1490C>G (p.Ala497Gly)not specified [RCV004605427]uncertain significance11113743823113743823Humanname
407493766CV3421152single nucleotide variantNM_004724.4(ZW10):c.1384G>C (p.Glu462Gln)not specified [RCV004605428]uncertain significance11113743929113743929Humanname
597758554CV3646449single nucleotide variantNM_004724.4(ZW10):c.1432C>G (p.Arg478Gly)not specified [RCV004894342]uncertain significance11113743881113743881Humanname
597758565CV3646451single nucleotide variantNM_004724.4(ZW10):c.1883A>G (p.Gln628Arg)not specified [RCV004894344]uncertain significance11113738265113738265Humanname
597758570CV3646452single nucleotide variantNM_004724.4(ZW10):c.1648C>G (p.His550Asp)not specified [RCV004894345]uncertain significance11113739318113739318Humanname
597758580CV3646454single nucleotide variantNM_004724.4(ZW10):c.1041G>T (p.Leu347Phe)not specified [RCV004894347]uncertain significance11113748305113748305Humanname
597758585CV3646455single nucleotide variantNM_004724.4(ZW10):c.1585G>A (p.Glu529Lys)not specified [RCV004894348]uncertain significance11113739381113739381Humanname
597758591CV3646456single nucleotide variantNM_004724.4(ZW10):c.1300C>A (p.Pro434Thr)not specified [RCV004894349]uncertain significance11113744013113744013Humanname
597758596CV3646457single nucleotide variantNM_004724.4(ZW10):c.2326G>C (p.Ala776Pro)not specified [RCV004894350]uncertain significance11113733708113733708Humanname
597758600CV3646458single nucleotide variantNM_004724.4(ZW10):c.1203C>A (p.Asn401Lys)not specified [RCV004894351]uncertain significance11113747600113747600Humanname
597758606CV3646459single nucleotide variantNM_004724.4(ZW10):c.1432C>A (p.Arg478Ser)not specified [RCV004894352]uncertain significance11113743881113743881Humanname
597758611CV3646460single nucleotide variantNM_004724.4(ZW10):c.2320G>A (p.Ala774Thr)not specified [RCV004894353]uncertain significance11113733714113733714Humanname
598276505CV3938447single nucleotide variantNM_004724.4(ZW10):c.1549C>T (p.His517Tyr)not specified [RCV005305639]uncertain significance11113741728113741728Humanname
598276507CV3938449single nucleotide variantNM_004724.4(ZW10):c.2186T>C (p.Met729Thr)not specified [RCV005305641]uncertain significance11113736653113736653Humanname
598201198CV3938452single nucleotide variantNM_004724.4(ZW10):c.2095C>T (p.Pro699Ser)not specified [RCV005314187]uncertain significance11113736744113736744Humanname
8626904CV82048single nucleotide variantNM_004724.3(ZW10):c.2107G>A (p.Glu703Lys)Malignant melanoma [RCV000062127]not provided11113736732113736732Humanname
8633854CV89070single nucleotide variantNM_004724.3(ZW10):c.1462G>C (p.Glu488Gln)Malignant melanoma [RCV000069167]not provided11113743851113743851Humanname