Arhgap18 Variant Search Result - Rat Genome Database

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61 records found for search term Arhgap18

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8626090	CV81234	single nucleotide variant	NM_033515.2(ARHGAP18):c.787-1G>T	Malignant melanoma [RCV000061312]	not provided	6	129618853	129618853	Human		name
156106804	CV2257303	single nucleotide variant	NM_033515.3(ARHGAP18):c.56G>A (p.Gly19Asp)	not specified [RCV004125408]	uncertain significance	6	129710081	129710081	Human		name
156361503	CV2269257	single nucleotide variant	NM_033515.3(ARHGAP18):c.91G>A (p.Ala31Thr)	not specified [RCV004130405]	uncertain significance	6	129710046	129710046	Human		name
155958814	CV2313838	single nucleotide variant	NM_033515.3(ARHGAP18):c.81C>A (p.Ser27Arg)	not specified [RCV004164159]	uncertain significance	6	129710056	129710056	Human		name
401920920	CV2820697	single nucleotide variant	NM_033515.3(ARHGAP18):c.462G>A (p.Thr154=)	not provided [RCV003432044]	likely benign	6	129638484	129638484	Human		name
405273260	CV3210365	deletion	NM_033515.3(ARHGAP18):c.1123-20_1123-13del	ARHGAP18-related disorder [RCV003914589]	likely benign	6	129608065	129608072	Human		name , trait , alternate_id
405684482	CV3286470	single nucleotide variant	NM_033515.3(ARHGAP18):c.73G>C (p.Gly25Arg)	not specified [RCV004422431]	uncertain significance	6	129710064	129710064	Human		name
598168278	CV4003236	single nucleotide variant	NM_033515.3(ARHGAP18):c.82C>T (p.His28Tyr)	not specified [RCV005391861]	uncertain significance	6	129710055	129710055	Human		name
15133825	CV710172	single nucleotide variant	NM_033515.3(ARHGAP18):c.94G>A (p.Gly32Arg)	not provided [RCV000965020]	benign	6	129710043	129710043	Human		name
156123372	CV2276171	single nucleotide variant	NM_033515.3(ARHGAP18):c.124G>A (p.Gly42Ser)	not specified [RCV004141830]	uncertain significance	6	129642008	129642008	Human		name
156171626	CV2355005	single nucleotide variant	NM_033515.3(ARHGAP18):c.116G>A (p.Arg39His)	not specified [RCV004198406]	uncertain significance	6	129642016	129642016	Human		name
401920918	CV2820696	single nucleotide variant	NM_033515.3(ARHGAP18):c.1113T>C (p.Ile371=)	not provided [RCV003432043]	likely benign	6	129611542	129611542	Human		name
405684443	CV3286461	single nucleotide variant	NM_033515.3(ARHGAP18):c.125G>A (p.Gly42Asp)	not specified [RCV004422422]	uncertain significance	6	129642007	129642007	Human		name
407531686	CV3471878	single nucleotide variant	NM_033515.3(ARHGAP18):c.203A>C (p.Asp68Ala)	not specified [RCV004657733]	uncertain significance	6	129641929	129641929	Human		name
597744008	CV3590666	single nucleotide variant	NM_033515.3(ARHGAP18):c.232T>C (p.Tyr78His)	not specified [RCV004845149]	uncertain significance	6	129641900	129641900	Human		name
598168154	CV4003212	single nucleotide variant	NM_033515.3(ARHGAP18):c.238A>C (p.Ile80Leu)	not specified [RCV005391838]	uncertain significance	6	129641894	129641894	Human		name
156365485	CV2272118	single nucleotide variant	NM_033515.3(ARHGAP18):c.845A>G (p.Gln282Arg)	not specified [RCV004124901]	uncertain significance	6	129618794	129618794	Human		name
156105496	CV2307397	single nucleotide variant	NM_033515.3(ARHGAP18):c.761G>C (p.Ser254Thr)	not specified [RCV004166077]	uncertain significance	6	129629378	129629378	Human		name
156305544	CV2338833	single nucleotide variant	NM_033515.3(ARHGAP18):c.983C>T (p.Ala328Val)	not specified [RCV004182388]	likely benign	6	129616273	129616273	Human		name
156041164	CV2342108	single nucleotide variant	NM_033515.3(ARHGAP18):c.908G>A (p.Gly303Asp)	not specified [RCV004191703]	uncertain significance	6	129618731	129618731	Human		name
155920280	CV2343324	single nucleotide variant	NM_033515.3(ARHGAP18):c.970G>A (p.Val324Ile)	not specified [RCV004194940]	likely benign	6	129616286	129616286	Human		name
156209553	CV2370129	single nucleotide variant	NM_033515.3(ARHGAP18):c.370G>A (p.Gly124Arg)	not specified [RCV004211015]	uncertain significance	6	129638576	129638576	Human		name
156347729	CV2382961	single nucleotide variant	NM_033515.3(ARHGAP18):c.424C>T (p.Arg142Trp)	not specified [RCV004217551]	uncertain significance	6	129638522	129638522	Human		name
156204887	CV2385124	single nucleotide variant	NM_033515.3(ARHGAP18):c.604C>G (p.Gln202Glu)	not specified [RCV004228384]	uncertain significance	6	129634054	129634054	Human		name
329396399	CV2462632	single nucleotide variant	NM_033515.3(ARHGAP18):c.385G>C (p.Asp129His)	not specified [RCV004278574]	uncertain significance	6	129638561	129638561	Human		name
401887238	CV2773257	single nucleotide variant	NM_033515.3(ARHGAP18):c.392A>G (p.Gln131Arg)	not specified [RCV004353929]	uncertain significance	6	129638554	129638554	Human		name
401883869	CV2785789	single nucleotide variant	NM_033515.3(ARHGAP18):c.995A>G (p.Gln332Arg)	not specified [RCV004365036]	uncertain significance	6	129616261	129616261	Human		name
405684471	CV3286467	single nucleotide variant	NM_033515.3(ARHGAP18):c.556C>G (p.Pro186Ala)	not specified [RCV004422428]	uncertain significance	6	129634102	129634102	Human		name
405684475	CV3286468	single nucleotide variant	NM_033515.3(ARHGAP18):c.574C>G (p.Gln192Glu)	not specified [RCV004422429]	uncertain significance	6	129634084	129634084	Human		name
405684477	CV3286469	single nucleotide variant	NM_033515.3(ARHGAP18):c.725A>G (p.Asn242Ser)	not specified [RCV004422430]	uncertain significance	6	129629414	129629414	Human		name
405684488	CV3286471	single nucleotide variant	NM_033515.3(ARHGAP18):c.784C>A (p.Pro262Thr)	not specified [RCV004422432]	uncertain significance	6	129629355	129629355	Human		name
405684492	CV3286472	single nucleotide variant	NM_033515.3(ARHGAP18):c.901G>A (p.Val301Ile)	not specified [RCV004422433]	uncertain significance	6	129618738	129618738	Human		name
407531699	CV3471887	single nucleotide variant	NM_033515.3(ARHGAP18):c.832G>A (p.Asp278Asn)	not specified [RCV004657739]	uncertain significance	6	129618807	129618807	Human		name
597744002	CV3590661	single nucleotide variant	NM_033515.3(ARHGAP18):c.670C>A (p.Pro224Thr)	not specified [RCV004845148]	uncertain significance	6	129629469	129629469	Human		name
597744142	CV3590692	single nucleotide variant	NM_033515.3(ARHGAP18):c.369C>A (p.Phe123Leu)	not specified [RCV004845174]	uncertain significance	6	129638577	129638577	Human		name
597744240	CV3590716	single nucleotide variant	NM_033515.3(ARHGAP18):c.745G>A (p.Glu249Lys)	not specified [RCV004845192]	uncertain significance	6	129629394	129629394	Human		name
597744289	CV3590727	single nucleotide variant	NM_033515.3(ARHGAP18):c.362A>G (p.Asn121Ser)	not specified [RCV004845201]	uncertain significance	6	129638584	129638584	Human		name
598168336	CV3999986	single nucleotide variant	NM_033515.3(ARHGAP18):c.656C>T (p.Pro219Leu)	not specified [RCV005391874]	likely benign	6	129629483	129629483	Human		name
598168111	CV4003200	single nucleotide variant	NM_033515.3(ARHGAP18):c.758A>C (p.Lys253Thr)	not specified [RCV005391829]	uncertain significance	6	129629381	129629381	Human		name
156333891	CV2214677	single nucleotide variant	NM_033515.3(ARHGAP18):c.1376A>C (p.Glu459Ala)	not specified [RCV004090499]	uncertain significance	6	129600838	129600838	Human		name
155950747	CV2302059	single nucleotide variant	NM_033515.3(ARHGAP18):c.1334T>C (p.Leu445Pro)	not specified [RCV004158820]	uncertain significance	6	129605908	129605908	Human		name
156388856	CV2376164	single nucleotide variant	NM_033515.3(ARHGAP18):c.1447G>A (p.Ala483Thr)	not specified [RCV004220393]	uncertain significance	6	129600767	129600767	Human		name
156083889	CV2395085	single nucleotide variant	NM_033515.3(ARHGAP18):c.1739G>A (p.Arg580Gln)	not specified [RCV004236768]	uncertain significance	6	129584087	129584087	Human		name
329353635	CV2466965	single nucleotide variant	NM_033515.3(ARHGAP18):c.1198G>A (p.Ala400Thr)	not specified [RCV004282717]	uncertain significance	6	129607977	129607977	Human		name
401881863	CV2774638	single nucleotide variant	NM_033515.3(ARHGAP18):c.1906C>T (p.Arg636Cys)	not specified [RCV004350105]	uncertain significance	6	129578599	129578599	Human		name
401898346	CV2787696	single nucleotide variant	NM_033515.3(ARHGAP18):c.1665G>C (p.Met555Ile)	not specified [RCV004356618]	uncertain significance	6	129599264	129599264	Human		name
405684432	CV3286459	single nucleotide variant	NM_033515.3(ARHGAP18):c.1031T>C (p.Leu344Ser)	not specified [RCV004422420]	uncertain significance	6	129616225	129616225	Human		name
405684446	CV3286462	single nucleotide variant	NM_033515.3(ARHGAP18):c.1303C>A (p.Gln435Lys)	not specified [RCV004422423]	uncertain significance	6	129605939	129605939	Human		name
405684450	CV3286463	single nucleotide variant	NM_033515.3(ARHGAP18):c.1708A>G (p.Asn570Asp)	not specified [RCV004422424]	uncertain significance	6	129599221	129599221	Human		name
405684455	CV3286464	single nucleotide variant	NM_033515.3(ARHGAP18):c.1907G>A (p.Arg636His)	not specified [RCV004422425]	uncertain significance	6	129578598	129578598	Human		name
405684466	CV3286466	single nucleotide variant	NM_033515.3(ARHGAP18):c.1941A>T (p.Leu647Phe)	not specified [RCV004422427]	uncertain significance	6	129578564	129578564	Human		name
407531670	CV3471868	single nucleotide variant	NM_033515.3(ARHGAP18):c.1676G>A (p.Arg559Gln)	not specified [RCV004657725]	uncertain significance	6	129599253	129599253	Human		name
597744050	CV3590675	single nucleotide variant	NM_033515.3(ARHGAP18):c.1055G>A (p.Arg352Gln)	not specified [RCV004845157]	uncertain significance	6	129611600	129611600	Human		name
597744099	CV3590684	single nucleotide variant	NM_033515.3(ARHGAP18):c.1958A>G (p.Asn653Ser)	not specified [RCV004845166]	uncertain significance	6	129578547	129578547	Human		name
597744148	CV3590697	single nucleotide variant	NM_033515.3(ARHGAP18):c.1037T>G (p.Phe346Cys)	not specified [RCV004845175]	uncertain significance	6	129616219	129616219	Human		name
597744191	CV3590706	single nucleotide variant	NM_033515.3(ARHGAP18):c.1613C>T (p.Thr538Met)	not specified [RCV004845183]	uncertain significance	6	129599316	129599316	Human		name
597744309	CV3590734	single nucleotide variant	NM_033515.3(ARHGAP18):c.1355A>G (p.Asp452Gly)	not specified [RCV004845205]	uncertain significance	6	129605887	129605887	Human		name
598205697	CV3999977	single nucleotide variant	NM_033515.3(ARHGAP18):c.1423G>C (p.Val475Leu)	not specified [RCV005399505]	uncertain significance	6	129600791	129600791	Human		name
598168083	CV4003194	single nucleotide variant	NM_033515.3(ARHGAP18):c.1055G>C (p.Arg352Pro)	not specified [RCV005391824]	uncertain significance	6	129611600	129611600	Human		name
598168204	CV4003222	single nucleotide variant	NM_033515.3(ARHGAP18):c.1547T>A (p.Ile516Asn)	not specified [RCV005391847]	uncertain significance	6	129600667	129600667	Human		name
598168249	CV4003230	single nucleotide variant	NM_033515.3(ARHGAP18):c.1256A>G (p.Tyr419Cys)	not specified [RCV005391855]	uncertain significance	6	129607919	129607919	Human		name

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