Rassf1 Variant Search Result - Rat Genome Database

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90 records found for search term Rassf1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401926441	CV2827447	single nucleotide variant	NM_007182.5(RASSF1):c.357+630C>T	not provided [RCV003437859]	likely benign	3	50337275	50337275	Human		name
401772977	CV2709053	single nucleotide variant	NM_007182.5(RASSF1):c.74G>A (p.Arg25Gln)	not specified [RCV004314397]	uncertain significance	3	50340732	50340732	Human		name
597784226	CV3589319	single nucleotide variant	NM_007182.5(RASSF1):c.91G>A (p.Ala31Thr)	not specified [RCV004854428]	uncertain significance	3	50340715	50340715	Human		name
15150747	CV708945	single nucleotide variant	NM_007182.5(RASSF1):c.753C>T (p.His251=)	not provided [RCV000968003]	benign	3	50331566	50331566	Human		name
15158081	CV734168	single nucleotide variant	NM_007182.5(RASSF1):c.483A>G (p.Thr161=)	not provided [RCV000902662]	benign	3	50331836	50331836	Human		name
8625642	CV80766	single nucleotide variant	NM_170714.1(RASSF1):c.969C>T (p.Ile323=)	Malignant melanoma [RCV000060843]	not provided	3	50330647	50330647	Human		name
156336672	CV2270873	single nucleotide variant	NM_007182.5(RASSF1):c.182C>G (p.Thr61Arg)	not specified [RCV004131915]	uncertain significance	3	50340624	50340624	Human		name
597784230	CV3589320	single nucleotide variant	NM_007182.5(RASSF1):c.131G>A (p.Arg44Gln)	not specified [RCV004854429]	uncertain significance	3	50340675	50340675	Human		name
597707023	CV3589322	single nucleotide variant	NM_007182.5(RASSF1):c.134A>G (p.Gln45Arg)	not specified [RCV004860566]	uncertain significance	3	50340672	50340672	Human		name
597784237	CV3589324	single nucleotide variant	NM_007182.5(RASSF1):c.280C>T (p.Arg94Cys)	not specified [RCV004854431]	uncertain significance	3	50337982	50337982	Human		name
597784245	CV3589329	single nucleotide variant	NM_007182.5(RASSF1):c.130C>G (p.Arg44Gly)	not specified [RCV004854433]	uncertain significance	3	50340676	50340676	Human		name
598185127	CV3902259	single nucleotide variant	NM_007182.5(RASSF1):c.235G>A (p.Gly79Ser)	not specified [RCV005265862]	uncertain significance	3	50340571	50340571	Human		name
156173017	CV2194312	single nucleotide variant	NM_007182.5(RASSF1):c.740G>A (p.Arg247His)	not specified [RCV004079427]	uncertain significance	3	50331579	50331579	Human		name
155966316	CV2216642	single nucleotide variant	NM_007182.5(RASSF1):c.784G>C (p.Asp262His)	not specified [RCV004083099]	uncertain significance	3	50331426	50331426	Human		name
156333576	CV2220856	single nucleotide variant	NM_007182.5(RASSF1):c.692G>A (p.Arg231Gln)	not specified [RCV004092286]	uncertain significance	3	50331627	50331627	Human		name
155997865	CV2260915	single nucleotide variant	NM_007182.5(RASSF1):c.699C>G (p.Phe233Leu)	not specified [RCV004125804]	uncertain significance	3	50331620	50331620	Human		name
155906736	CV2357375	single nucleotide variant	NM_007182.5(RASSF1):c.799C>T (p.Arg267Trp)	not specified [RCV004200261]	uncertain significance	3	50331411	50331411	Human		name
156042832	CV2387889	single nucleotide variant	NM_007182.5(RASSF1):c.883G>A (p.Ala295Thr)	not specified [RCV004236440]	uncertain significance	3	50330721	50330721	Human		name
329356159	CV2442483	single nucleotide variant	NM_007182.5(RASSF1):c.677T>C (p.Ile226Thr)	not specified [RCV004266724]	uncertain significance	3	50331642	50331642	Human		name
401728794	CV2673049	single nucleotide variant	NM_007182.5(RASSF1):c.566G>A (p.Arg189Gln)	not specified [RCV004284038]	uncertain significance	3	50331753	50331753	Human		name
401779168	CV2733193	single nucleotide variant	NM_007182.5(RASSF1):c.572G>A (p.Gly191Asp)	not specified [RCV004332116]	uncertain significance	3	50331747	50331747	Human		name
401865378	CV2778734	single nucleotide variant	NM_007182.5(RASSF1):c.980G>A (p.Arg327His)	not specified [RCV004346645]	uncertain significance	3	50330624	50330624	Human		name
405660190	CV3312460	single nucleotide variant	NM_007182.5(RASSF1):c.526G>A (p.Val176Met)	not specified [RCV004438780]	uncertain significance	3	50331793	50331793	Human		name
407467031	CV3468634	single nucleotide variant	NM_007182.5(RASSF1):c.949C>T (p.Arg317Cys)	not specified [RCV004660617]	uncertain significance	3	50330655	50330655	Human		name
407467035	CV3468635	single nucleotide variant	NM_007182.5(RASSF1):c.719G>A (p.Arg240His)	not specified [RCV004660618]	uncertain significance	3	50331600	50331600	Human		name
407467039	CV3468636	single nucleotide variant	NM_007182.5(RASSF1):c.748C>T (p.Arg250Cys)	not specified [RCV004660619]	uncertain significance	3	50331571	50331571	Human		name
407467043	CV3468637	single nucleotide variant	NM_007182.5(RASSF1):c.364C>A (p.Pro122Thr)	not specified [RCV004660620]	uncertain significance	3	50332148	50332148	Human		name
597707014	CV3589321	single nucleotide variant	NM_007182.5(RASSF1):c.668G>A (p.Arg223His)	not specified [RCV004860565]	uncertain significance	3	50331651	50331651	Human		name
597784233	CV3589323	single nucleotide variant	NM_007182.5(RASSF1):c.742G>A (p.Ala248Thr)	not specified [RCV004854430]	uncertain significance	3	50331577	50331577	Human		name
597707033	CV3589325	single nucleotide variant	NM_007182.5(RASSF1):c.655C>A (p.Arg219Ser)	not specified [RCV004860567]	uncertain significance	3	50331664	50331664	Human		name
597707041	CV3589327	single nucleotide variant	NM_007182.5(RASSF1):c.586A>C (p.Thr196Pro)	not specified [RCV004860568]	uncertain significance	3	50331733	50331733	Human		name
597707050	CV3589328	single nucleotide variant	NM_007182.5(RASSF1):c.786T>G (p.Asp262Glu)	not specified [RCV004860569]	uncertain significance	3	50331424	50331424	Human		name
598185121	CV3902258	single nucleotide variant	NM_007182.5(RASSF1):c.662G>A (p.Arg221Lys)	not specified [RCV005265861]	uncertain significance	3	50331657	50331657	Human		name
156182419	CV2243035	single nucleotide variant	NM_007182.5(RASSF1):c.1001T>C (p.Leu334Pro)	not specified [RCV004109954]	uncertain significance	3	50330603	50330603	Human		name
405660187	CV3312459	single nucleotide variant	NM_007182.5(RASSF1):c.1005C>G (p.His335Gln)	not specified [RCV004438779]	uncertain significance	3	50330599	50330599	Human		name
155922108	CV2284272	single nucleotide variant	NM_001080521.3(RASSF10):c.10T>C (p.Ser4Pro)	not specified [RCV004146630]	uncertain significance	11	13009586	13009586	Human		name
598185182	CV3902268	single nucleotide variant	NM_001080521.3(RASSF10):c.67T>C (p.Ser23Pro)	not specified [RCV005265871]	uncertain significance	11	13009643	13009643	Human		name
156006195	CV2357747	single nucleotide variant	NM_001080521.3(RASSF10):c.236T>C (p.Leu79Pro)	not specified [RCV004205041]	uncertain significance	11	13009812	13009812	Human		name
156248820	CV2394014	single nucleotide variant	NM_001080521.3(RASSF10):c.179G>A (p.Gly60Asp)	not specified [RCV004236234]	uncertain significance	11	13009755	13009755	Human		name
401898084	CV2780952	single nucleotide variant	NM_001080521.3(RASSF10):c.161C>T (p.Ser54Leu)	not specified [RCV004354486]	uncertain significance	11	13009737	13009737	Human		name
405660202	CV3312464	single nucleotide variant	NM_001080521.3(RASSF10):c.251T>A (p.Leu84Gln)	not specified [RCV004438784]	uncertain significance	11	13009827	13009827	Human		name
597784248	CV3589331	single nucleotide variant	NM_001080521.3(RASSF10):c.223G>T (p.Asp75Tyr)	not specified [RCV004854434]	uncertain significance	11	13009799	13009799	Human		name
598185134	CV3902260	single nucleotide variant	NM_001080521.3(RASSF10):c.215A>G (p.Asp72Gly)	not specified [RCV005265863]	uncertain significance	11	13009791	13009791	Human		name
598185153	CV3902263	single nucleotide variant	NM_001080521.3(RASSF10):c.228C>G (p.Asp76Glu)	not specified [RCV005265866]	uncertain significance	11	13009804	13009804	Human		name
598185172	CV3902266	single nucleotide variant	NM_001080521.3(RASSF10):c.199C>G (p.Pro67Ala)	not specified [RCV005265869]	uncertain significance	11	13009775	13009775	Human		name
155985724	CV2233916	single nucleotide variant	NM_001080521.3(RASSF10):c.980A>C (p.Asp327Ala)	not specified [RCV004104269]	uncertain significance	11	13010556	13010556	Human		name
155916227	CV2239686	single nucleotide variant	NM_001080521.3(RASSF10):c.913G>A (p.Ala305Thr)	not specified [RCV004108231]	uncertain significance	11	13010489	13010489	Human		name
156197067	CV2241594	single nucleotide variant	NM_001080521.3(RASSF10):c.757A>G (p.Ile253Val)	not specified [RCV004104480]	uncertain significance	11	13010333	13010333	Human		name
156084914	CV2244579	single nucleotide variant	NM_001080521.3(RASSF10):c.506C>G (p.Thr169Ser)	not specified [RCV004102307]	uncertain significance	11	13010082	13010082	Human		name
156254712	CV2264672	single nucleotide variant	NM_001080521.3(RASSF10):c.303G>C (p.Glu101Asp)	not specified [RCV004132671]	uncertain significance	11	13009879	13009879	Human		name
156266998	CV2329646	single nucleotide variant	NM_001080521.3(RASSF10):c.670C>G (p.Arg224Gly)	not specified [RCV004180758]	uncertain significance	11	13010246	13010246	Human		name
156044473	CV2381635	single nucleotide variant	NM_001080521.3(RASSF10):c.711C>G (p.His237Gln)	not specified [RCV004232106]	uncertain significance	11	13010287	13010287	Human		name
155960887	CV2390778	single nucleotide variant	NM_001080521.3(RASSF10):c.482C>G (p.Pro161Arg)	not specified [RCV004241064]	uncertain significance	11	13010058	13010058	Human		name
329358917	CV2425442	single nucleotide variant	NM_001080521.3(RASSF10):c.355G>A (p.Glu119Lys)	not specified [RCV004251097]	uncertain significance	11	13009931	13009931	Human		name
401775453	CV2692379	single nucleotide variant	NM_001080521.3(RASSF10):c.631T>C (p.Ser211Pro)	not specified [RCV004310356]	uncertain significance	11	13010207	13010207	Human		name
401880454	CV2763046	single nucleotide variant	NM_001080521.3(RASSF10):c.386T>G (p.Val129Gly)	not specified [RCV004336104]	uncertain significance	11	13009962	13009962	Human		name
405660208	CV3312466	single nucleotide variant	NM_001080521.3(RASSF10):c.412G>T (p.Ala138Ser)	not specified [RCV004438786]	uncertain significance	11	13009988	13009988	Human		name
405660211	CV3312467	single nucleotide variant	NM_001080521.3(RASSF10):c.419C>T (p.Pro140Leu)	not specified [RCV004438787]	uncertain significance	11	13009995	13009995	Human		name
405660214	CV3312468	single nucleotide variant	NM_001080521.3(RASSF10):c.437G>C (p.Arg146Pro)	not specified [RCV004438788]	uncertain significance	11	13010013	13010013	Human		name
405660217	CV3312469	single nucleotide variant	NM_001080521.3(RASSF10):c.587C>T (p.Pro196Leu)	not specified [RCV004438789]	uncertain significance	11	13010163	13010163	Human		name
405660220	CV3312470	single nucleotide variant	NM_001080521.3(RASSF10):c.734G>A (p.Arg245Gln)	not specified [RCV004438790]	uncertain significance	11	13010310	13010310	Human		name
407467047	CV3468638	single nucleotide variant	NM_001080521.3(RASSF10):c.482C>A (p.Pro161Gln)	not specified [RCV004660621]	uncertain significance	11	13010058	13010058	Human		name
407467060	CV3468641	single nucleotide variant	NM_001080521.3(RASSF10):c.881C>T (p.Pro294Leu)	not specified [RCV004660624]	uncertain significance	11	13010457	13010457	Human		name
407467064	CV3468642	single nucleotide variant	NM_001080521.3(RASSF10):c.880C>T (p.Pro294Ser)	not specified [RCV004660625]	uncertain significance	11	13010456	13010456	Human		name
597707059	CV3589330	single nucleotide variant	NM_001080521.3(RASSF10):c.334C>A (p.Arg112Ser)	not specified [RCV004860570]	uncertain significance	11	13009910	13009910	Human		name
597707064	CV3589332	single nucleotide variant	NM_001080521.3(RASSF10):c.326G>A (p.Arg109His)	not specified [RCV004860571]	uncertain significance	11	13009902	13009902	Human		name
597784252	CV3589335	single nucleotide variant	NM_001080521.3(RASSF10):c.832T>A (p.Leu278Met)	not specified [RCV004854435]	uncertain significance	11	13010408	13010408	Human		name
597784259	CV3589337	single nucleotide variant	NM_001080521.3(RASSF10):c.756G>C (p.Glu252Asp)	not specified [RCV004854437]	uncertain significance	11	13010332	13010332	Human		name
597784264	CV3589338	single nucleotide variant	NM_001080521.3(RASSF10):c.751C>T (p.Arg251Cys)	not specified [RCV004854438]	uncertain significance	11	13010327	13010327	Human		name
597707090	CV3589339	single nucleotide variant	NM_001080521.3(RASSF10):c.906G>T (p.Glu302Asp)	not specified [RCV004860574]	uncertain significance	11	13010482	13010482	Human		name
597707098	CV3589340	single nucleotide variant	NM_001080521.3(RASSF10):c.421C>T (p.Arg141Cys)	not specified [RCV004860575]	uncertain significance	11	13009997	13009997	Human		name
597784272	CV3589342	single nucleotide variant	NM_001080521.3(RASSF10):c.863C>G (p.Ser288Cys)	not specified [RCV004854440]	uncertain significance	11	13010439	13010439	Human		name
598185140	CV3902261	single nucleotide variant	NM_001080521.3(RASSF10):c.673A>G (p.Met225Val)	not specified [RCV005265864]	uncertain significance	11	13010249	13010249	Human		name
598185147	CV3902262	single nucleotide variant	NM_001080521.3(RASSF10):c.454G>C (p.Glu152Gln)	not specified [RCV005265865]	uncertain significance	11	13010030	13010030	Human		name
598185160	CV3902264	single nucleotide variant	NM_001080521.3(RASSF10):c.722A>G (p.Gln241Arg)	not specified [RCV005265867]	uncertain significance	11	13010298	13010298	Human		name
598185165	CV3902265	single nucleotide variant	NM_001080521.3(RASSF10):c.865A>G (p.Arg289Gly)	not specified [RCV005265868]	uncertain significance	11	13010441	13010441	Human		name
156163858	CV2246708	single nucleotide variant	NM_001080521.3(RASSF10):c.1269C>G (p.Asp423Glu)	not specified [RCV004110430]	uncertain significance	11	13010845	13010845	Human		name
156071302	CV2251404	single nucleotide variant	NM_001080521.3(RASSF10):c.1180C>T (p.Leu394Phe)	not specified [RCV004117388]	uncertain significance	11	13010756	13010756	Human		name
156177872	CV2317281	single nucleotide variant	NM_001080521.3(RASSF10):c.1231G>A (p.Val411Ile)	not specified [RCV004178772]	uncertain significance	11	13010807	13010807	Human		name
405660196	CV3312462	single nucleotide variant	NM_001080521.3(RASSF10):c.1276A>C (p.Lys426Gln)	not specified [RCV004438782]	uncertain significance	11	13010852	13010852	Human		name
405660199	CV3312463	single nucleotide variant	NM_001080521.3(RASSF10):c.1397T>G (p.Met466Arg)	not specified [RCV004438783]	uncertain significance	11	13010973	13010973	Human		name
407467055	CV3468640	single nucleotide variant	NM_001080521.3(RASSF10):c.1516C>T (p.Leu506Phe)	not specified [RCV004660623]	uncertain significance	11	13011092	13011092	Human		name
407467068	CV3468643	single nucleotide variant	NM_001080521.3(RASSF10):c.1412C>T (p.Ala471Val)	not specified [RCV004660626]	uncertain significance	11	13010988	13010988	Human		name
597707073	CV3589333	single nucleotide variant	NM_001080521.3(RASSF10):c.1431C>A (p.Ser477Arg)	not specified [RCV004860572]	uncertain significance	11	13011007	13011007	Human		name
597707082	CV3589334	single nucleotide variant	NM_001080521.3(RASSF10):c.1072T>C (p.Trp358Arg)	not specified [RCV004860573]	uncertain significance	11	13010648	13010648	Human		name
597784268	CV3589341	single nucleotide variant	NM_001080521.3(RASSF10):c.1439G>A (p.Gly480Asp)	not specified [RCV004854439]	uncertain significance	11	13011015	13011015	Human		name
597707105	CV3589343	single nucleotide variant	NM_001080521.3(RASSF10):c.1432G>A (p.Gly478Ser)	not specified [RCV004860576]	uncertain significance	11	13011008	13011008	Human		name
598185177	CV3902267	single nucleotide variant	NM_001080521.3(RASSF10):c.1135C>T (p.Pro379Ser)	not specified [RCV005265870]	uncertain significance	11	13010711	13010711	Human		name
598185189	CV3902269	single nucleotide variant	NM_001080521.3(RASSF10):c.1139A>G (p.Asp380Gly)	not specified [RCV005265872]	uncertain significance	11	13010715	13010715	Human		name
598185196	CV3902270	single nucleotide variant	NM_001080521.3(RASSF10):c.1195T>C (p.Tyr399His)	not specified [RCV005265873]	uncertain significance	11	13010771	13010771	Human		name

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