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43 records found for search term Klhl18
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156034111CV2275193single nucleotide variantNM_025010.5(KLHL18):c.17C>T (p.Ala6Val)not specified [RCV004136988]uncertain significance34728298247282982Humanname
156315830CV2250829single nucleotide variantNM_025010.5(KLHL18):c.64A>G (p.Ser22Gly)not specified [RCV004129687]uncertain significance34728302947283029Humanname
156203995CV2252453single nucleotide variantNM_025010.5(KLHL18):c.61C>T (p.Pro21Ser)not specified [RCV004116574]uncertain significance34728302647283026Humanname
401740220CV2683294single nucleotide variantNM_025010.5(KLHL18):c.37G>A (p.Val13Met)not specified [RCV004288075]uncertain significance34728300247283002Humanname
597639905CV3692334single nucleotide variantNM_025010.5(KLHL18):c.71G>C (p.Gly24Ala)not specified [RCV004941439]uncertain significance34728303647283036Humanname
401757027CV2678192single nucleotide variantNM_025010.5(KLHL18):c.115G>A (p.Asp39Asn)not specified [RCV004296699]uncertain significance34728308047283080Humanname
597639886CV3692330single nucleotide variantNM_025010.5(KLHL18):c.262G>T (p.Ala88Ser)not specified [RCV004941436]uncertain significance34732256947322569Humanname
156095144CV2253007single nucleotide variantNM_025010.5(KLHL18):c.550G>A (p.Val184Met)not specified [RCV004120807]uncertain significance34733009947330099Humanname
156336493CV2333680single nucleotide variantNM_025010.5(KLHL18):c.376G>A (p.Ala126Thr)not specified [RCV004192518]uncertain significance34732268347322683Humanname
155990949CV2372116single nucleotide variantNM_025010.5(KLHL18):c.583G>A (p.Val195Ile)not specified [RCV004221774]uncertain significance34733013247330132Humanname
401741183CV2680348single nucleotide variantNM_025010.5(KLHL18):c.653C>A (p.Pro218His)not specified [RCV004288598]uncertain significance34733320947333209Humanname
401737201CV2699697single nucleotide variantNM_025010.5(KLHL18):c.559C>A (p.Leu187Met)not specified [RCV004299865]uncertain significance34733010847330108Humanname
401899823CV2758878single nucleotide variantNM_025010.5(KLHL18):c.472G>A (p.Ala158Thr)not specified [RCV004339966]uncertain significance34733002147330021Humanname
405808004CV3265765single nucleotide variantNM_025010.5(KLHL18):c.451A>T (p.Met151Leu)not specified [RCV004406836]uncertain significance34733000047330000Humanname
405808006CV3265766single nucleotide variantNM_025010.5(KLHL18):c.569G>A (p.Arg190Gln)not specified [RCV004406837]uncertain significance34733011847330118Humanname
405808008CV3265767single nucleotide variantNM_025010.5(KLHL18):c.688C>A (p.Pro230Thr)not specified [RCV004406838]uncertain significance34733324447333244Humanname
405808010CV3265768single nucleotide variantNM_025010.5(KLHL18):c.716A>G (p.Asp239Gly)not specified [RCV004406839]uncertain significance34733327247333272Humanname
405808011CV3265769single nucleotide variantNM_025010.5(KLHL18):c.806G>A (p.Arg269His)not specified [RCV004406840]uncertain significance34733472747334727Humanname
405808013CV3265770single nucleotide variantNM_025010.5(KLHL18):c.941A>G (p.Asn314Ser)not specified [RCV004406841]uncertain significance34733657747336577Humanname
407470493CV3448518single nucleotide variantNM_025010.5(KLHL18):c.928G>A (p.Asp310Asn)not specified [RCV004637121]uncertain significance34733656447336564Humanname
407470497CV3448520single nucleotide variantNM_025010.5(KLHL18):c.613G>T (p.Ala205Ser)not specified [RCV004637122]uncertain significance34733316947333169Humanname
407470506CV3448522single nucleotide variantNM_025010.5(KLHL18):c.982C>T (p.Arg328Cys)not specified [RCV004637124]uncertain significance34733661847336618Humanname
597639893CV3692332single nucleotide variantNM_025010.5(KLHL18):c.427G>A (p.Val143Met)not specified [RCV004941437]uncertain significance34732997647329976Humanname
597639912CV3692335single nucleotide variantNM_025010.5(KLHL18):c.656A>G (p.Tyr219Cys)not specified [RCV004941440]likely benign34733321247333212Humanname
598182681CV3976759single nucleotide variantNM_025010.5(KLHL18):c.431G>A (p.Arg144His)not specified [RCV005352774]uncertain significance34732998047329980Humanname
329387042CV2452808single nucleotide variantNM_025010.5(KLHL18):c.1592G>T (p.Gly531Val)not specified [RCV004275339]uncertain significance34734380847343808Humanname
401877338CV2790134single nucleotide variantNM_025010.5(KLHL18):c.1123G>A (p.Ala375Thr)not specified [RCV004364072]uncertain significance34734057347340573Humanname
405807994CV3265760single nucleotide variantNM_025010.5(KLHL18):c.1112G>A (p.Ser371Asn)not specified [RCV004406831]uncertain significance34733674847336748Humanname
405807997CV3265761single nucleotide variantNM_025010.5(KLHL18):c.1174G>C (p.Asp392His)not specified [RCV004406832]uncertain significance34734062447340624Humanname
405807998CV3265762single nucleotide variantNM_025010.5(KLHL18):c.1220C>T (p.Thr407Met)not specified [RCV004406833]uncertain significance34734067047340670Humanname
405808000CV3265763single nucleotide variantNM_025010.5(KLHL18):c.1582G>A (p.Ala528Thr)not specified [RCV004406834]uncertain significance34734379847343798Humanname
405808002CV3265764single nucleotide variantNM_025010.5(KLHL18):c.1663G>A (p.Ala555Thr)not specified [RCV004406835]uncertain significance34734387947343879Humanname
407524931CV3448517single nucleotide variantNM_025010.5(KLHL18):c.1456G>A (p.Asp486Asn)not specified [RCV004631550]uncertain significance34734367247343672Humanname
407525052CV3448519single nucleotide variantNM_025010.5(KLHL18):c.1315G>C (p.Asp439His)not specified [RCV004631551]uncertain significance34734280747342807Humanname
407470501CV3448521single nucleotide variantNM_025010.5(KLHL18):c.1006G>C (p.Gly336Arg)not specified [RCV004637123]uncertain significance34733664247336642Humanname
597639900CV3692333single nucleotide variantNM_025010.5(KLHL18):c.1373A>G (p.His458Arg)not specified [RCV004941438]uncertain significance34734358947343589Humanname
597768696CV3692336single nucleotide variantNM_025010.5(KLHL18):c.1292G>C (p.Arg431Thr)not specified [RCV004927544]uncertain significance34734278447342784Humanname
598182674CV3976758single nucleotide variantNM_025010.5(KLHL18):c.1546C>T (p.Arg516Trp)not specified [RCV005352773]uncertain significance34734376247343762Humanname
598182687CV3976760single nucleotide variantNM_025010.5(KLHL18):c.1390C>T (p.Leu464Phe)not specified [RCV005352775]uncertain significance34734360647343606Humanname
598182694CV3987291single nucleotide variantNM_025010.5(KLHL18):c.1535C>T (p.Thr512Met)not specified [RCV005352776]uncertain significance34734375147343751Humanname
598182701CV3987292single nucleotide variantNM_025010.5(KLHL18):c.1562C>T (p.Ala521Val)not specified [RCV005352777]uncertain significance34734377847343778Humanname
598182707CV3987293single nucleotide variantNM_025010.5(KLHL18):c.1558G>C (p.Val520Leu)not specified [RCV005352778]uncertain significance34734377447343774Humanname
598161452CV3987294single nucleotide variantNM_025010.5(KLHL18):c.1669A>G (p.Met557Val)not specified [RCV005368437]uncertain significance34734388547343885Humanname