Rbm19 Variant Search Result - Rat Genome Database

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116 records found for search term Rbm19

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
598253412	CV3898703	single nucleotide variant	NM_016196.4(RBM19):c.17T>C (p.Val6Ala)	not specified [RCV005259581]	uncertain significance	12	113966211	113966211	Human		name
405670562	CV3308896	single nucleotide variant	NM_016196.4(RBM19):c.33T>G (p.Asn11Lys)	not specified [RCV004441177]	uncertain significance	12	113966195	113966195	Human		name
405670582	CV3308900	single nucleotide variant	NM_016196.4(RBM19):c.57G>T (p.Arg19Ser)	not specified [RCV004441181]	uncertain significance	12	113962394	113962394	Human		name
405670600	CV3308903	single nucleotide variant	NM_016196.4(RBM19):c.71C>T (p.Ala24Val)	not specified [RCV004441184]	uncertain significance	12	113962380	113962380	Human		name
156075385	CV2350875	single nucleotide variant	NM_016196.4(RBM19):c.191A>G (p.Lys64Arg)	not specified [RCV004211712]	likely benign	12	113962260	113962260	Human		name
156169691	CV2354809	single nucleotide variant	NM_016196.4(RBM19):c.118A>G (p.Lys40Glu)	not specified [RCV004198336]	uncertain significance	12	113962333	113962333	Human		name
405670510	CV3308886	single nucleotide variant	NM_016196.4(RBM19):c.211C>T (p.Arg71Trp)	not specified [RCV004441167]	uncertain significance	12	113962240	113962240	Human		name
407507362	CV3468887	single nucleotide variant	NM_016196.4(RBM19):c.170A>G (p.Lys57Arg)	not specified [RCV004671697]	uncertain significance	12	113962281	113962281	Human		name
597784998	CV3585909	single nucleotide variant	NM_016196.4(RBM19):c.241G>A (p.Gly81Arg)	not specified [RCV004854619]	uncertain significance	12	113960157	113960157	Human		name
597727755	CV3585917	single nucleotide variant	NM_016196.4(RBM19):c.278C>T (p.Ala93Val)	not specified [RCV004862716]	uncertain significance	12	113960120	113960120	Human		name
597785022	CV3585920	single nucleotide variant	NM_016196.4(RBM19):c.109A>G (p.Lys37Glu)	not specified [RCV004854625]	uncertain significance	12	113962342	113962342	Human		name
597785039	CV3585928	single nucleotide variant	NM_016196.4(RBM19):c.267G>C (p.Trp89Cys)	not specified [RCV004854629]	uncertain significance	12	113960131	113960131	Human		name
598253299	CV3898686	single nucleotide variant	NM_016196.4(RBM19):c.211C>G (p.Arg71Gly)	not specified [RCV005259564]	uncertain significance	12	113962240	113962240	Human		name
598253332	CV3898691	single nucleotide variant	NM_016196.4(RBM19):c.226T>C (p.Phe76Leu)	not specified [RCV005259569]	uncertain significance	12	113960172	113960172	Human		name
598253347	CV3898693	single nucleotide variant	NM_016196.4(RBM19):c.107C>T (p.Thr36Ile)	not specified [RCV005259571]	uncertain significance	12	113962344	113962344	Human		name
598253434	CV3898706	single nucleotide variant	NM_016196.4(RBM19):c.193A>C (p.Ser65Arg)	not specified [RCV005259584]	uncertain significance	12	113962258	113962258	Human		name
155949706	CV2267703	single nucleotide variant	NM_016196.4(RBM19):c.518A>G (p.Asp173Gly)	not specified [RCV004134240]	uncertain significance	12	113959265	113959265	Human		name
156269401	CV2275697	single nucleotide variant	NM_016196.4(RBM19):c.464A>G (p.Asp155Gly)	not specified [RCV004137310]	uncertain significance	12	113959319	113959319	Human		name
156278898	CV2316718	single nucleotide variant	NM_016196.4(RBM19):c.370C>G (p.Leu124Val)	not specified [RCV004171942]	uncertain significance	12	113959873	113959873	Human		name
155980873	CV2336971	single nucleotide variant	NM_016196.4(RBM19):c.860A>C (p.Gln287Pro)	not specified [RCV004192744]	uncertain significance	12	113955192	113955192	Human		name
156064246	CV2349773	single nucleotide variant	NM_016196.4(RBM19):c.652G>C (p.Ala218Pro)	not specified [RCV004204185]	uncertain significance	12	113957970	113957970	Human		name
156154293	CV2369491	single nucleotide variant	NM_016196.4(RBM19):c.391A>G (p.Thr131Ala)	not specified [RCV004210428]	uncertain significance	12	113959392	113959392	Human		name
156260667	CV2395565	single nucleotide variant	NM_016196.4(RBM19):c.617C>T (p.Ser206Leu)	not specified [RCV004241418]	uncertain significance	12	113958005	113958005	Human		name
401721884	CV2710216	single nucleotide variant	NM_016196.4(RBM19):c.650A>G (p.Lys217Arg)	not specified [RCV004317116]	uncertain significance	12	113957972	113957972	Human		name
405670558	CV3308895	single nucleotide variant	NM_016196.4(RBM19):c.315C>A (p.Asp105Glu)	not specified [RCV004441176]	uncertain significance	12	113960083	113960083	Human		name
405670568	CV3308897	single nucleotide variant	NM_016196.4(RBM19):c.357G>T (p.Lys119Asn)	not specified [RCV004441178]	uncertain significance	12	113959886	113959886	Human		name
405670570	CV3308898	single nucleotide variant	NM_016196.4(RBM19):c.494C>T (p.Pro165Leu)	not specified [RCV004441179]	uncertain significance	12	113959289	113959289	Human		name
405670576	CV3308899	single nucleotide variant	NM_016196.4(RBM19):c.520T>G (p.Ser174Ala)	not specified [RCV004441180]	uncertain significance	12	113959263	113959263	Human		name
405670594	CV3308902	single nucleotide variant	NM_016196.4(RBM19):c.693T>G (p.Asp231Glu)	not specified [RCV004441183]	uncertain significance	12	113957929	113957929	Human		name
405670606	CV3308904	single nucleotide variant	NM_016196.4(RBM19):c.745G>A (p.Ala249Thr)	not specified [RCV004441185]	likely benign	12	113957877	113957877	Human		name
405670609	CV3308905	single nucleotide variant	NM_016196.4(RBM19):c.905C>T (p.Pro302Leu)	not specified [RCV004441186]	uncertain significance	12	113955147	113955147	Human		name
407507359	CV3468883	single nucleotide variant	NM_016196.4(RBM19):c.710A>T (p.Asp237Val)	not specified [RCV004671696]	uncertain significance	12	113957912	113957912	Human		name
597785011	CV3585914	single nucleotide variant	NM_016196.4(RBM19):c.625G>C (p.Asp209His)	not specified [RCV004854622]	uncertain significance	12	113957997	113957997	Human		name
597727765	CV3585918	single nucleotide variant	NM_016196.4(RBM19):c.572A>G (p.Glu191Gly)	not specified [RCV004862717]	uncertain significance	12	113958050	113958050	Human		name
597785020	CV3585919	single nucleotide variant	NM_016196.4(RBM19):c.649A>G (p.Lys217Glu)	not specified [RCV004854624]	uncertain significance	12	113957973	113957973	Human		name
598253306	CV3898687	single nucleotide variant	NM_016196.4(RBM19):c.986A>G (p.His329Arg)	not specified [RCV005259565]	uncertain significance	12	113952526	113952526	Human		name
598253320	CV3898689	single nucleotide variant	NM_016196.4(RBM19):c.310A>G (p.Lys104Glu)	not specified [RCV005259567]	uncertain significance	12	113960088	113960088	Human		name
598253326	CV3898690	single nucleotide variant	NM_016196.4(RBM19):c.586G>A (p.Glu196Lys)	not specified [RCV005259568]	uncertain significance	12	113958036	113958036	Human		name
598253359	CV3898695	single nucleotide variant	NM_016196.4(RBM19):c.998C>T (p.Thr333Ile)	not specified [RCV005259573]	uncertain significance	12	113952514	113952514	Human		name
598253405	CV3898702	single nucleotide variant	NM_016196.4(RBM19):c.793C>G (p.Gln265Glu)	not specified [RCV005259580]	uncertain significance	12	113957829	113957829	Human		name
156081058	CV2195388	single nucleotide variant	NM_016196.4(RBM19):c.1598A>G (p.Asn533Ser)	not specified [RCV004080301]	likely benign	12	113945856	113945856	Human		name
156136407	CV2196172	single nucleotide variant	NM_016196.4(RBM19):c.2432G>A (p.Arg811Gln)	not specified [RCV004073530]	uncertain significance	12	113918401	113918401	Human		name
156229005	CV2209278	single nucleotide variant	NM_016196.4(RBM19):c.2532C>G (p.His844Gln)	not specified [RCV004091679]	uncertain significance	12	113914995	113914995	Human		name
155977475	CV2226413	single nucleotide variant	NM_016196.4(RBM19):c.2155G>A (p.Glu719Lys)	not specified [RCV004099631]	uncertain significance	12	113927143	113927143	Human		name
156239394	CV2235917	single nucleotide variant	NM_016196.4(RBM19):c.2308G>A (p.Val770Met)	not specified [RCV004113805]	uncertain significance	12	113920688	113920688	Human		name
156070346	CV2251329	single nucleotide variant	NM_016196.4(RBM19):c.1642G>A (p.Val548Met)	not specified [RCV004115537]	uncertain significance	12	113942419	113942419	Human		name
155980106	CV2263618	single nucleotide variant	NM_016196.4(RBM19):c.1691G>A (p.Arg564Gln)	not specified [RCV004135622]	uncertain significance	12	113942370	113942370	Human		name
156293503	CV2293063	single nucleotide variant	NM_016196.4(RBM19):c.2472A>C (p.Gln824His)	not specified [RCV004148810]	uncertain significance	12	113915055	113915055	Human		name
155941404	CV2294244	single nucleotide variant	NM_016196.4(RBM19):c.1958A>C (p.Tyr653Ser)	not specified [RCV004149593]	uncertain significance	12	113937117	113937117	Human		name
156080377	CV2301001	single nucleotide variant	NM_016196.4(RBM19):c.1173G>T (p.Glu391Asp)	not specified [RCV004158164]	uncertain significance	12	113948936	113948936	Human		name
156072736	CV2325357	single nucleotide variant	NM_016196.4(RBM19):c.1108G>A (p.Val370Ile)	not specified [RCV004177736]	uncertain significance	12	113949001	113949001	Human		name
156056973	CV2326708	single nucleotide variant	NM_016196.4(RBM19):c.1879G>T (p.Val627Leu)	not specified [RCV004185284]	uncertain significance	12	113940019	113940019	Human		name
155974894	CV2342603	single nucleotide variant	NM_016196.4(RBM19):c.1576G>A (p.Asp526Asn)	not specified [RCV004196694]	uncertain significance	12	113945878	113945878	Human		name
155984166	CV2344714	single nucleotide variant	NM_016196.4(RBM19):c.2585G>A (p.Arg862His)	not specified [RCV004190872]	uncertain significance	12	113858870	113858870	Human		name
155981732	CV2351407	single nucleotide variant	NM_016196.4(RBM19):c.2656G>C (p.Asp886His)	not specified [RCV004193097]	uncertain significance	12	113858799	113858799	Human		name
156102961	CV2352329	single nucleotide variant	NM_016196.4(RBM19):c.2821G>A (p.Glu941Lys)	not specified [RCV004200802]	uncertain significance	12	113823286	113823286	Human		name
155924862	CV2358225	single nucleotide variant	NM_016196.4(RBM19):c.1690C>T (p.Arg564Trp)	not specified [RCV004212018]	uncertain significance	12	113942371	113942371	Human		name
156384082	CV2361809	single nucleotide variant	NM_016196.4(RBM19):c.1061G>A (p.Arg354Gln)	not specified [RCV004223280]	uncertain significance	12	113950094	113950094	Human		name
156043813	CV2397050	single nucleotide variant	NM_016196.4(RBM19):c.2510G>A (p.Arg837Gln)	not specified [RCV004236565]	uncertain significance	12	113915017	113915017	Human		name
329402828	CV2451386	single nucleotide variant	NM_016196.4(RBM19):c.1465A>G (p.Ser489Gly)	not specified [RCV004272070]	uncertain significance	12	113946418	113946418	Human		name
329376962	CV2456758	single nucleotide variant	NM_016196.4(RBM19):c.2234A>C (p.Lys745Thr)	not specified [RCV004270735]	likely benign	12	113927064	113927064	Human		name
329371483	CV2458141	single nucleotide variant	NM_016196.4(RBM19):c.2024C>T (p.Thr675Ile)	not specified [RCV004271952]	uncertain significance	12	113937051	113937051	Human		name
401745148	CV2681201	single nucleotide variant	NM_016196.4(RBM19):c.1082A>G (p.Tyr361Cys)	not specified [RCV004289342]	uncertain significance	12	113949027	113949027	Human		name
401762219	CV2699561	single nucleotide variant	NM_016196.4(RBM19):c.2413G>C (p.Glu805Gln)	not specified [RCV004299760]	uncertain significance	12	113918420	113918420	Human		name
401757563	CV2707851	single nucleotide variant	NM_016196.4(RBM19):c.1456G>A (p.Glu486Lys)	not specified [RCV004309131]	uncertain significance	12	113946427	113946427	Human		name
401751091	CV2715863	single nucleotide variant	NM_016196.4(RBM19):c.1536C>G (p.His512Gln)	not specified [RCV004328977]	uncertain significance	12	113945918	113945918	Human		name
401857646	CV2756226	single nucleotide variant	NM_016196.4(RBM19):c.2392G>A (p.Val798Ile)	not specified [RCV004338322]	likely benign	12	113918441	113918441	Human		name
401860799	CV2758635	single nucleotide variant	NM_016196.4(RBM19):c.2629G>A (p.Gly877Ser)	not specified [RCV004337709]	uncertain significance	12	113858826	113858826	Human		name
401894833	CV2785362	single nucleotide variant	NM_016196.4(RBM19):c.1508A>G (p.Gln503Arg)	not specified [RCV004357111]	uncertain significance	12	113946375	113946375	Human		name
405670466	CV3308877	single nucleotide variant	NM_016196.4(RBM19):c.1006A>G (p.Ile336Val)	not specified [RCV004441158]	likely benign	12	113950149	113950149	Human		name
405670472	CV3308878	single nucleotide variant	NM_016196.4(RBM19):c.1087G>A (p.Glu363Lys)	not specified [RCV004441159]	uncertain significance	12	113949022	113949022	Human		name
405670478	CV3308879	single nucleotide variant	NM_016196.4(RBM19):c.1298A>G (p.Tyr433Cys)	not specified [RCV004441160]	uncertain significance	12	113947443	113947443	Human		name
405670483	CV3308880	single nucleotide variant	NM_016196.4(RBM19):c.1301C>T (p.Pro434Leu)	not specified [RCV004441161]	uncertain significance	12	113947440	113947440	Human		name
405670488	CV3308881	single nucleotide variant	NM_016196.4(RBM19):c.1420C>T (p.His474Tyr)	not specified [RCV004441162]	uncertain significance	12	113946463	113946463	Human		name
405670497	CV3308883	single nucleotide variant	NM_016196.4(RBM19):c.1442A>G (p.Lys481Arg)	not specified [RCV004441164]	uncertain significance	12	113946441	113946441	Human		name
405670502	CV3308884	single nucleotide variant	NM_016196.4(RBM19):c.1684G>A (p.Glu562Lys)	not specified [RCV004441165]	uncertain significance	12	113942377	113942377	Human		name
405670505	CV3308885	single nucleotide variant	NM_016196.4(RBM19):c.2080G>A (p.Glu694Lys)	not specified [RCV004441166]	uncertain significance	12	113927218	113927218	Human		name
405670516	CV3308887	single nucleotide variant	NM_016196.4(RBM19):c.2161G>A (p.Glu721Lys)	not specified [RCV004441168]	uncertain significance	12	113927137	113927137	Human		name
405670520	CV3308888	single nucleotide variant	NM_016196.4(RBM19):c.2176A>G (p.Ser726Gly)	not specified [RCV004441169]	uncertain significance	12	113927122	113927122	Human		name
405670526	CV3308889	single nucleotide variant	NM_016196.4(RBM19):c.2185G>C (p.Gly729Arg)	not specified [RCV004441170]	uncertain significance	12	113927113	113927113	Human		name
405670532	CV3308890	single nucleotide variant	NM_016196.4(RBM19):c.2449G>A (p.Val817Met)	not specified [RCV004441171]	uncertain significance	12	113915078	113915078	Human		name
405670536	CV3308891	single nucleotide variant	NM_016196.4(RBM19):c.2571G>C (p.Glu857Asp)	not specified [RCV004441172]	uncertain significance	12	113858884	113858884	Human		name
405670541	CV3308892	single nucleotide variant	NM_016196.4(RBM19):c.2666G>A (p.Arg889Lys)	not specified [RCV004441173]	uncertain significance	12	113844787	113844787	Human		name
405670547	CV3308893	single nucleotide variant	NM_016196.4(RBM19):c.2753C>G (p.Ala918Gly)	not specified [RCV004441174]	uncertain significance	12	113844700	113844700	Human		name
405670552	CV3308894	single nucleotide variant	NM_016196.4(RBM19):c.2758C>T (p.Arg920Trp)	not specified [RCV004441175]	uncertain significance	12	113844695	113844695	Human		name
407507356	CV3468881	single nucleotide variant	NM_016196.4(RBM19):c.2002C>G (p.Gln668Glu)	not specified [RCV004671695]	uncertain significance	12	113937073	113937073	Human		name
407468016	CV3468882	single nucleotide variant	NM_016196.4(RBM19):c.1176C>A (p.Asn392Lys)	not specified [RCV004660799]	uncertain significance	12	113948933	113948933	Human		name
407468015	CV3468884	single nucleotide variant	NM_016196.4(RBM19):c.2282T>A (p.Ile761Asn)	not specified [RCV004660800]	uncertain significance	12	113924720	113924720	Human		name
407468013	CV3468885	single nucleotide variant	NM_016196.4(RBM19):c.1582A>G (p.Ile528Val)	not specified [RCV004660801]	uncertain significance	12	113945872	113945872	Human		name
407468011	CV3468886	single nucleotide variant	NM_016196.4(RBM19):c.1933T>G (p.Ser645Ala)	not specified [RCV004660802]	uncertain significance	12	113939965	113939965	Human		name
597727729	CV3585908	single nucleotide variant	NM_016196.4(RBM19):c.1843C>T (p.Arg615Cys)	not specified [RCV004862713]	uncertain significance	12	113940055	113940055	Human		name
597785002	CV3585910	single nucleotide variant	NM_016196.4(RBM19):c.2164G>A (p.Glu722Lys)	not specified [RCV004854620]	uncertain significance	12	113927134	113927134	Human		name
597727739	CV3585911	single nucleotide variant	NM_016196.4(RBM19):c.2515A>C (p.Ile839Leu)	not specified [RCV004862714]	uncertain significance	12	113915012	113915012	Human		name
597785008	CV3585912	single nucleotide variant	NM_016196.4(RBM19):c.1247A>G (p.Glu416Gly)	not specified [RCV004854621]	uncertain significance	12	113948862	113948862	Human		name
597785015	CV3585915	single nucleotide variant	NM_016196.4(RBM19):c.2803C>T (p.Arg935Trp)	not specified [RCV004854623]	uncertain significance	12	113823304	113823304	Human		name
597727748	CV3585916	single nucleotide variant	NM_016196.4(RBM19):c.1538A>G (p.Asn513Ser)	not specified [RCV004862715]	uncertain significance	12	113945916	113945916	Human		name
597727773	CV3585921	single nucleotide variant	NM_016196.4(RBM19):c.1876A>C (p.Ile626Leu)	not specified [RCV004862718]	uncertain significance	12	113940022	113940022	Human		name
597727782	CV3585922	single nucleotide variant	NM_016196.4(RBM19):c.2063A>G (p.Glu688Gly)	not specified [RCV004862719]	uncertain significance	12	113937012	113937012	Human		name
597785026	CV3585924	single nucleotide variant	NM_016196.4(RBM19):c.2182C>T (p.Pro728Ser)	not specified [RCV004854626]	uncertain significance	12	113927116	113927116	Human		name
597727790	CV3585925	single nucleotide variant	NM_016196.4(RBM19):c.1739C>G (p.Ala580Gly)	not specified [RCV004862720]	uncertain significance	12	113940159	113940159	Human		name
597785031	CV3585926	single nucleotide variant	NM_016196.4(RBM19):c.2308G>C (p.Val770Leu)	not specified [RCV004854627]	uncertain significance	12	113920688	113920688	Human		name
597785036	CV3585927	single nucleotide variant	NM_016196.4(RBM19):c.2579C>T (p.Thr860Met)	not specified [RCV004854628]	uncertain significance	12	113858876	113858876	Human		name
598253312	CV3898688	single nucleotide variant	NM_016196.4(RBM19):c.1654G>A (p.Val552Met)	not specified [RCV005259566]	uncertain significance	12	113942407	113942407	Human		name
598253338	CV3898692	single nucleotide variant	NM_016196.4(RBM19):c.1711G>A (p.Gly571Arg)	not specified [RCV005259570]	uncertain significance	12	113942350	113942350	Human		name
598253354	CV3898694	single nucleotide variant	NM_016196.4(RBM19):c.1969G>C (p.Ala657Pro)	not specified [RCV005259572]	uncertain significance	12	113937106	113937106	Human		name
598253365	CV3898696	single nucleotide variant	NM_016196.4(RBM19):c.1423G>A (p.Val475Met)	not specified [RCV005259574]	uncertain significance	12	113946460	113946460	Human		name
598253371	CV3898697	single nucleotide variant	NM_016196.4(RBM19):c.2351C>T (p.Pro784Leu)	not specified [RCV005259575]	uncertain significance	12	113920645	113920645	Human		name
598253378	CV3898698	single nucleotide variant	NM_016196.4(RBM19):c.1030G>C (p.Glu344Gln)	not specified [RCV005259576]	uncertain significance	12	113950125	113950125	Human		name
598253386	CV3898699	single nucleotide variant	NM_016196.4(RBM19):c.1376C>T (p.Ala459Val)	not specified [RCV005259577]	uncertain significance	12	113947365	113947365	Human		name
598253394	CV3898700	single nucleotide variant	NM_016196.4(RBM19):c.2842G>C (p.Gly948Arg)	not specified [RCV005259578]	uncertain significance	12	113823265	113823265	Human		name
598253399	CV3898701	single nucleotide variant	NM_016196.4(RBM19):c.1069A>G (p.Met357Val)	not specified [RCV005259579]	uncertain significance	12	113950086	113950086	Human		name
598253422	CV3898704	single nucleotide variant	NM_016196.4(RBM19):c.1004A>G (p.Tyr335Cys)	not specified [RCV005259582]	uncertain significance	12	113950151	113950151	Human		name
598253428	CV3898705	single nucleotide variant	NM_016196.4(RBM19):c.1243G>A (p.Glu415Lys)	not specified [RCV005259583]	uncertain significance	12	113948866	113948866	Human		name
8627189	CV82333	single nucleotide variant	NM_001146698.1(RBM19):c.516C>T (p.Phe172=)	Malignant melanoma [RCV000062412]	not provided	12	113959267	113959267	Human		name
8653542	CV130117	single nucleotide variant	NM_001146698.1(RBM19):c.2385G>A (p.Gln795=)	Lung cancer [RCV000110604]	uncertain significance	12	113920611	113920611	Human		name
8634513	CV89733	single nucleotide variant	NM_001146698.1(RBM19):c.343G>A (p.Glu115Lys)	Malignant melanoma [RCV000069830]	not provided	12	113959900	113959900	Human		name

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