Stk11ip Variant Search Result - Rat Genome Database

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133 records found for search term Stk11ip

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597747522	CV3614817	single nucleotide variant	NM_052902.4(STK11IP):c.-30T>G	not specified [RCV004866081]	likely benign	2	219597920	219597920	Human		name
597747538	CV3614821	single nucleotide variant	NM_052902.4(STK11IP):c.-26G>A	not specified [RCV004866084]	uncertain significance	2	219598094	219598094	Human		name
156167697	CV2270504	single nucleotide variant	NM_052902.4(STK11IP):c.19G>A (p.Asp7Asn)	not specified [RCV004137463]	uncertain significance	2	219598138	219598138	Human		name
156147136	CV2381837	single nucleotide variant	NM_052902.4(STK11IP):c.10G>A (p.Ala4Thr)	not specified [RCV004232280]	uncertain significance	2	219598129	219598129	Human		name
329361617	CV2437698	single nucleotide variant	NM_052902.4(STK11IP):c.25C>G (p.Leu9Val)	not specified [RCV004261011]	uncertain significance	2	219598144	219598144	Human		name
597794464	CV3614810	single nucleotide variant	NM_052902.4(STK11IP):c.20A>T (p.Asp7Val)	not specified [RCV004877861]	uncertain significance	2	219598139	219598139	Human		name
156191780	CV2223132	single nucleotide variant	NM_052902.4(STK11IP):c.57G>C (p.Glu19Asp)	not specified [RCV004103979]	uncertain significance	2	219598176	219598176	Human		name
156290827	CV2226237	single nucleotide variant	NM_052902.4(STK11IP):c.40G>C (p.Ala14Pro)	not specified [RCV004099491]	uncertain significance	2	219598159	219598159	Human		name
405741485	CV3334452	single nucleotide variant	NM_052902.4(STK11IP):c.41C>G (p.Ala14Gly)	not specified [RCV004465665]	uncertain significance	2	219598160	219598160	Human		name
597794467	CV3614818	single nucleotide variant	NM_052902.4(STK11IP):c.58T>G (p.Ser20Ala)	not specified [RCV004877862]	uncertain significance	2	219598177	219598177	Human		name
156123632	CV2234066	single nucleotide variant	NM_052902.4(STK11IP):c.257T>C (p.Leu86Pro)	not specified [RCV004106172]	uncertain significance	2	219601430	219601430	Human		name
156386953	CV2364901	single nucleotide variant	NM_052902.4(STK11IP):c.214A>G (p.Ile72Val)	not specified [RCV004221802]	uncertain significance	2	219601387	219601387	Human		name
401860301	CV2762388	single nucleotide variant	NM_052902.4(STK11IP):c.274C>T (p.His92Tyr)	not specified [RCV004335495]	uncertain significance	2	219601647	219601647	Human		name
407496289	CV3485483	single nucleotide variant	NM_052902.4(STK11IP):c.283G>T (p.Gly95Cys)	not specified [RCV004668097]	uncertain significance	2	219601656	219601656	Human		name
598207393	CV3919661	single nucleotide variant	NM_052902.4(STK11IP):c.271G>A (p.Val91Ile)	not specified [RCV005291278]	uncertain significance	2	219601644	219601644	Human		name
156268558	CV2195024	single nucleotide variant	NM_052902.4(STK11IP):c.658C>T (p.Arg220Cys)	not specified [RCV004077944]	uncertain significance	2	219605647	219605647	Human		name
156180556	CV2258449	single nucleotide variant	NM_052902.4(STK11IP):c.964G>T (p.Val322Phe)	not specified [RCV004115642]	uncertain significance	2	219606494	219606494	Human		name
155921868	CV2284210	single nucleotide variant	NM_052902.4(STK11IP):c.506A>G (p.Asn169Ser)	not specified [RCV004146581]	uncertain significance	2	219602535	219602535	Human		name
156275685	CV2290697	single nucleotide variant	NM_052902.4(STK11IP):c.751G>A (p.Glu251Lys)	not specified [RCV004149221]	uncertain significance	2	219605961	219605961	Human		name
156293297	CV2306311	single nucleotide variant	NM_052902.4(STK11IP):c.518A>G (p.Asn173Ser)	not specified [RCV004163025]	uncertain significance	2	219602547	219602547	Human		name
155967189	CV2329887	single nucleotide variant	NM_052902.4(STK11IP):c.565C>T (p.Arg189Cys)	not specified [RCV004183345]	uncertain significance	2	219602723	219602723	Human		name
155923008	CV2340719	single nucleotide variant	NM_052902.4(STK11IP):c.304A>G (p.Ile102Val)	not specified [RCV004190389]	uncertain significance	2	219601677	219601677	Human		name
156341892	CV2368476	single nucleotide variant	NM_052902.4(STK11IP):c.659G>A (p.Arg220His)	not specified [RCV004221278]	likely benign	2	219605648	219605648	Human		name
156171754	CV2380734	single nucleotide variant	NM_052902.4(STK11IP):c.460G>A (p.Gly154Ser)	not specified [RCV004218306]	uncertain significance	2	219602489	219602489	Human		name
329378457	CV2446951	single nucleotide variant	NM_052902.4(STK11IP):c.694G>T (p.Ala232Ser)	not specified [RCV004257795]	uncertain significance	2	219605683	219605683	Human		name
329387022	CV2452789	single nucleotide variant	NM_052902.4(STK11IP):c.601T>C (p.Cys201Arg)	not specified [RCV004275324]	uncertain significance	2	219602759	219602759	Human		name
329377538	CV2453471	single nucleotide variant	NM_052902.4(STK11IP):c.845G>T (p.Arg282Leu)	not specified [RCV004267072]	uncertain significance	2	219606055	219606055	Human		name
401781007	CV2681858	single nucleotide variant	NM_052902.4(STK11IP):c.668T>C (p.Leu223Ser)	not specified [RCV004296852]	uncertain significance	2	219605657	219605657	Human		name
401781159	CV2681908	single nucleotide variant	NM_052902.4(STK11IP):c.868C>G (p.Pro290Ala)	not specified [RCV004296900]	uncertain significance	2	219606213	219606213	Human		name
401778379	CV2709072	single nucleotide variant	NM_052902.4(STK11IP):c.325T>A (p.Ser109Thr)	not specified [RCV004314410]	uncertain significance	2	219601698	219601698	Human		name
401870002	CV2772590	single nucleotide variant	NM_052902.4(STK11IP):c.719G>A (p.Arg240Gln)	not specified [RCV004355345]	uncertain significance	2	219605708	219605708	Human		name
405741521	CV3334447	single nucleotide variant	NM_052902.4(STK11IP):c.331C>T (p.Arg111Trp)	not specified [RCV004465660]	uncertain significance	2	219601704	219601704	Human		name
405741514	CV3334448	single nucleotide variant	NM_052902.4(STK11IP):c.442C>T (p.Leu148Phe)	not specified [RCV004465661]	uncertain significance	2	219602471	219602471	Human		name
405741505	CV3334449	single nucleotide variant	NM_052902.4(STK11IP):c.566G>A (p.Arg189His)	not specified [RCV004465662]	uncertain significance	2	219602724	219602724	Human		name
405741493	CV3334451	single nucleotide variant	NM_052902.4(STK11IP):c.640C>A (p.Leu214Met)	not specified [RCV004465664]	uncertain significance	2	219605629	219605629	Human		name
405741477	CV3334453	single nucleotide variant	NM_052902.4(STK11IP):c.770G>A (p.Arg257Gln)	not specified [RCV004465666]	uncertain significance	2	219605980	219605980	Human		name
405741472	CV3334454	single nucleotide variant	NM_052902.4(STK11IP):c.943G>T (p.Gly315Cys)	not specified [RCV004465667]	uncertain significance	2	219606288	219606288	Human		name
407496292	CV3485484	single nucleotide variant	NM_052902.4(STK11IP):c.845G>A (p.Arg282His)	not specified [RCV004668098]	uncertain significance	2	219606055	219606055	Human		name
407496305	CV3485491	single nucleotide variant	NM_052902.4(STK11IP):c.808C>T (p.Arg270Trp)	not specified [RCV004668102]	uncertain significance	2	219606018	219606018	Human		name
597747492	CV3614809	single nucleotide variant	NM_052902.4(STK11IP):c.733C>T (p.Arg245Trp)	not specified [RCV004866075]	uncertain significance	2	219605722	219605722	Human		name
597747497	CV3614811	single nucleotide variant	NM_052902.4(STK11IP):c.995C>T (p.Thr332Ile)	not specified [RCV004866076]	uncertain significance	2	219606719	219606719	Human		name
597747501	CV3614812	single nucleotide variant	NM_052902.4(STK11IP):c.847A>C (p.Lys283Gln)	not specified [RCV004866077]	uncertain significance	2	219606057	219606057	Human		name
598207417	CV3919664	single nucleotide variant	NM_052902.4(STK11IP):c.430G>A (p.Ala144Thr)	not specified [RCV005291281]	likely benign	2	219602075	219602075	Human		name
156027253	CV2199305	single nucleotide variant	NM_052902.4(STK11IP):c.2312A>G (p.His771Arg)	not specified [RCV004082653]	likely benign	2	219611811	219611811	Human		name
156368004	CV2203633	single nucleotide variant	NM_052902.4(STK11IP):c.2297C>T (p.Pro766Leu)	not specified [RCV004073953]	likely benign	2	219611796	219611796	Human		name
156399445	CV2205122	single nucleotide variant	NM_052902.4(STK11IP):c.2774A>T (p.Glu925Val)	not specified [RCV004077720]	uncertain significance	2	219614218	219614218	Human		name
156326145	CV2209600	single nucleotide variant	NM_052902.4(STK11IP):c.1690G>C (p.Ala564Pro)	not specified [RCV004093697]	uncertain significance	2	219608669	219608669	Human		name
156253907	CV2209601	single nucleotide variant	NM_052902.4(STK11IP):c.1691C>T (p.Ala564Val)	not specified [RCV004093698]	uncertain significance	2	219608670	219608670	Human		name
156381436	CV2214943	single nucleotide variant	NM_052902.4(STK11IP):c.1321G>A (p.Gly441Arg)	not specified [RCV004084726]	uncertain significance	2	219608148	219608148	Human		name
156116481	CV2221709	single nucleotide variant	NM_052902.4(STK11IP):c.1882C>T (p.Arg628Cys)	not specified [RCV004098475]	uncertain significance	2	219609169	219609169	Human		name
156141553	CV2243851	single nucleotide variant	NM_052902.4(STK11IP):c.1885C>T (p.Arg629Cys)	not specified [RCV004114798]	uncertain significance	2	219609172	219609172	Human		name
155984746	CV2274728	single nucleotide variant	NM_052902.4(STK11IP):c.1168G>A (p.Glu390Lys)	not specified [RCV004139091]	uncertain significance	2	219607086	219607086	Human		name
156272049	CV2286521	single nucleotide variant	NM_052902.4(STK11IP):c.1078A>C (p.Ser360Arg)	not specified [RCV004140021]	uncertain significance	2	219606802	219606802	Human		name
156174837	CV2290398	single nucleotide variant	NM_052902.4(STK11IP):c.1912C>G (p.His638Asp)	not specified [RCV004154818]	uncertain significance	2	219609199	219609199	Human		name
156202702	CV2300661	single nucleotide variant	NM_052902.4(STK11IP):c.2479T>G (p.Cys827Gly)	not specified [RCV004155607]	uncertain significance	2	219613167	219613167	Human		name
156202994	CV2300688	single nucleotide variant	NM_052902.4(STK11IP):c.1672T>C (p.Phe558Leu)	not specified [RCV004155629]	uncertain significance	2	219608651	219608651	Human		name
156203008	CV2300689	single nucleotide variant	NM_052902.4(STK11IP):c.1673T>G (p.Phe558Cys)	not specified [RCV004155630]	uncertain significance	2	219608652	219608652	Human		name
156272057	CV2315872	single nucleotide variant	NM_052902.4(STK11IP):c.2995G>A (p.Val999Met)	not specified [RCV004171648]	uncertain significance	2	219615219	219615219	Human		name
156160581	CV2319390	single nucleotide variant	NM_052902.4(STK11IP):c.1315C>T (p.Pro439Ser)	not specified [RCV004184984]	uncertain significance	2	219608142	219608142	Human		name
156272404	CV2333923	single nucleotide variant	NM_052902.4(STK11IP):c.1241C>T (p.Pro414Leu)	not specified [RCV004183457]	uncertain significance	2	219608068	219608068	Human		name
156064440	CV2340759	single nucleotide variant	NM_052902.4(STK11IP):c.1640A>G (p.Glu547Gly)	not specified [RCV004188121]	uncertain significance	2	219608619	219608619	Human		name
156003365	CV2357448	single nucleotide variant	NM_052902.4(STK11IP):c.2600T>C (p.Ile867Thr)	not specified [RCV004202740]	uncertain significance	2	219613814	219613814	Human		name
156285057	CV2360740	single nucleotide variant	NM_052902.4(STK11IP):c.1808C>T (p.Thr603Met)	not specified [RCV004213526]	uncertain significance	2	219608787	219608787	Human		name
156340227	CV2363205	single nucleotide variant	NM_052902.4(STK11IP):c.1378T>G (p.Ser460Ala)	not specified [RCV004213771]	likely benign	2	219608205	219608205	Human		name
156199454	CV2365325	single nucleotide variant	NM_052902.4(STK11IP):c.2344C>T (p.Arg782Cys)	not specified [RCV004209411]	uncertain significance	2	219611963	219611963	Human		name
156155971	CV2367922	single nucleotide variant	NM_052902.4(STK11IP):c.1591A>G (p.Lys531Glu)	not specified [RCV004223019]	uncertain significance	2	219608418	219608418	Human		name
156390689	CV2383322	single nucleotide variant	NM_052902.4(STK11IP):c.1831G>A (p.Ala611Thr)	not specified [RCV004222364]	uncertain significance	2	219609118	219609118	Human		name
156213284	CV2385839	single nucleotide variant	NM_052902.4(STK11IP):c.1958A>G (p.Asn653Ser)	not specified [RCV004603406]	uncertain significance	2	219609394	219609394	Human		name
156039176	CV2390291	single nucleotide variant	NM_052902.4(STK11IP):c.2377C>T (p.Arg793Trp)	not specified [RCV004240657]	uncertain significance	2	219611996	219611996	Human		name
329380387	CV2466592	single nucleotide variant	NM_052902.4(STK11IP):c.1070C>T (p.Pro357Leu)	not specified [RCV004274120]	uncertain significance	2	219606794	219606794	Human		name
401729030	CV2673127	single nucleotide variant	NM_052902.4(STK11IP):c.1939G>A (p.Val647Met)	not specified [RCV004284110]	uncertain significance	2	219609375	219609375	Human		name
401721031	CV2673575	single nucleotide variant	NM_052902.4(STK11IP):c.1145G>A (p.Arg382His)	not specified [RCV004288537]	uncertain significance	2	219607063	219607063	Human		name
401752315	CV2682778	single nucleotide variant	NM_052902.4(STK11IP):c.2155G>A (p.Ala719Thr)	not specified [RCV004281751]	likely benign	2	219611654	219611654	Human		name
401775751	CV2692484	single nucleotide variant	NM_052902.4(STK11IP):c.2928T>G (p.Asp976Glu)	not specified [RCV004312236]	likely benign	2	219615152	219615152	Human		name
401745327	CV2693232	single nucleotide variant	NM_052902.4(STK11IP):c.1267C>T (p.Arg423Trp)	not specified [RCV004295206]	uncertain significance	2	219608094	219608094	Human		name
401731287	CV2693711	single nucleotide variant	NM_052902.4(STK11IP):c.1849C>T (p.Arg617Cys)	not specified [RCV004298039]	uncertain significance	2	219609136	219609136	Human		name
401769954	CV2710760	single nucleotide variant	NM_052902.4(STK11IP):c.2615C>T (p.Ala872Val)	not specified [RCV004308696]	uncertain significance	2	219613829	219613829	Human		name
401749605	CV2719337	single nucleotide variant	NM_052902.4(STK11IP):c.1946C>T (p.Thr649Ile)	not specified [RCV004324971]	uncertain significance	2	219609382	219609382	Human		name
401866651	CV2762710	single nucleotide variant	NM_052902.4(STK11IP):c.2329A>G (p.Ser777Gly)	not specified [RCV004340269]	uncertain significance	2	219611828	219611828	Human		name
401892173	CV2777298	single nucleotide variant	NM_052902.4(STK11IP):c.2246C>T (p.Pro749Leu)	not specified [RCV004354313]	uncertain significance	2	219611745	219611745	Human		name
405740676	CV3334427	single nucleotide variant	NM_052902.4(STK11IP):c.1052C>T (p.Pro351Leu)	not specified [RCV004465640]	uncertain significance	2	219606776	219606776	Human		name
405740685	CV3334428	single nucleotide variant	NM_052902.4(STK11IP):c.1075C>G (p.Leu359Val)	not specified [RCV004465641]	uncertain significance	2	219606799	219606799	Human		name
405740690	CV3334429	single nucleotide variant	NM_052902.4(STK11IP):c.1274G>A (p.Arg425Gln)	not specified [RCV004465642]	uncertain significance	2	219608101	219608101	Human		name
405740705	CV3334431	single nucleotide variant	NM_052902.4(STK11IP):c.1384G>A (p.Gly462Ser)	not specified [RCV004465644]	likely benign	2	219608211	219608211	Human		name
405740710	CV3334432	single nucleotide variant	NM_052902.4(STK11IP):c.1480C>T (p.Pro494Ser)	not specified [RCV004465645]	uncertain significance	2	219608307	219608307	Human		name
405740717	CV3334433	single nucleotide variant	NM_052902.4(STK11IP):c.1554G>C (p.Glu518Asp)	not specified [RCV004465646]	uncertain significance	2	219608381	219608381	Human		name
405740730	CV3334435	single nucleotide variant	NM_052902.4(STK11IP):c.1724G>A (p.Arg575His)	not specified [RCV004465648]	uncertain significance	2	219608703	219608703	Human		name
405740737	CV3334436	single nucleotide variant	NM_052902.4(STK11IP):c.1768A>C (p.Ile590Leu)	not specified [RCV004465649]	likely benign	2	219608747	219608747	Human		name
405741571	CV3334439	single nucleotide variant	NM_052902.4(STK11IP):c.2020C>T (p.Arg674Cys)	not specified [RCV004465652]	uncertain significance	2	219609456	219609456	Human		name
405741565	CV3334440	single nucleotide variant	NM_052902.4(STK11IP):c.2129G>A (p.Cys710Tyr)	not specified [RCV004465653]	uncertain significance	2	219611628	219611628	Human		name
405741560	CV3334441	single nucleotide variant	NM_052902.4(STK11IP):c.2357G>A (p.Arg786His)	not specified [RCV004465654]	uncertain significance	2	219611976	219611976	Human		name
405741549	CV3334443	single nucleotide variant	NM_052902.4(STK11IP):c.2851C>T (p.Arg951Trp)	not specified [RCV004465656]	uncertain significance	2	219614528	219614528	Human		name
407530118	CV3485485	single nucleotide variant	NM_052902.4(STK11IP):c.1519A>G (p.Lys507Glu)	not specified [RCV004681660]	likely benign	2	219608346	219608346	Human		name
407530119	CV3485486	single nucleotide variant	NM_052902.4(STK11IP):c.1718C>T (p.Ala573Val)	not specified [RCV004681661]	uncertain significance	2	219608697	219608697	Human		name
407530120	CV3485487	single nucleotide variant	NM_052902.4(STK11IP):c.2542C>A (p.Pro848Thr)	not specified [RCV004681662]	uncertain significance	2	219613756	219613756	Human		name
407496296	CV3485488	single nucleotide variant	NM_052902.4(STK11IP):c.1633C>T (p.Pro545Ser)	not specified [RCV004668099]	uncertain significance	2	219608612	219608612	Human		name
407496303	CV3485490	single nucleotide variant	NM_052902.4(STK11IP):c.1378T>C (p.Ser460Pro)	not specified [RCV004668101]	uncertain significance	2	219608205	219608205	Human		name
407496308	CV3485492	single nucleotide variant	NM_052902.4(STK11IP):c.2158G>T (p.Val720Leu)	not specified [RCV004668103]	likely benign	2	219611657	219611657	Human		name
597747456	CV3614801	single nucleotide variant	NM_052902.4(STK11IP):c.2356C>T (p.Arg786Cys)	not specified [RCV004866068]	uncertain significance	2	219611975	219611975	Human		name
597747461	CV3614802	single nucleotide variant	NM_052902.4(STK11IP):c.2288C>G (p.Pro763Arg)	not specified [RCV004866069]	uncertain significance	2	219611787	219611787	Human		name
597747466	CV3614803	single nucleotide variant	NM_052902.4(STK11IP):c.1723C>T (p.Arg575Cys)	not specified [RCV004866070]	uncertain significance	2	219608702	219608702	Human		name
597747471	CV3614804	single nucleotide variant	NM_052902.4(STK11IP):c.1153C>T (p.Arg385Trp)	not specified [RCV004866071]	uncertain significance	2	219607071	219607071	Human		name
597747477	CV3614805	single nucleotide variant	NM_052902.4(STK11IP):c.1238A>G (p.His413Arg)	not specified [RCV004866072]	uncertain significance	2	219608065	219608065	Human		name
597747482	CV3614806	single nucleotide variant	NM_052902.4(STK11IP):c.1415C>T (p.Pro472Leu)	not specified [RCV004866073]	likely benign	2	219608242	219608242	Human		name
597747487	CV3614807	single nucleotide variant	NM_052902.4(STK11IP):c.2329A>C (p.Ser777Arg)	not specified [RCV004866074]	uncertain significance	2	219611828	219611828	Human		name
597747506	CV3614813	single nucleotide variant	NM_052902.4(STK11IP):c.2980G>A (p.Glu994Lys)	not specified [RCV004866078]	uncertain significance	2	219615204	219615204	Human		name
597747517	CV3614815	single nucleotide variant	NM_052902.4(STK11IP):c.2587G>T (p.Asp863Tyr)	not specified [RCV004866080]	uncertain significance	2	219613801	219613801	Human		name
597747527	CV3614819	single nucleotide variant	NM_052902.4(STK11IP):c.1433G>C (p.Gly478Ala)	not specified [RCV004866082]	uncertain significance	2	219608260	219608260	Human		name
597747532	CV3614820	single nucleotide variant	NM_052902.4(STK11IP):c.1711C>T (p.Leu571Phe)	not specified [RCV004866083]	uncertain significance	2	219608690	219608690	Human		name
597747544	CV3614822	single nucleotide variant	NM_052902.4(STK11IP):c.1889A>G (p.Tyr630Cys)	not specified [RCV004866085]	uncertain significance	2	219609176	219609176	Human		name
597747549	CV3614823	single nucleotide variant	NM_052902.4(STK11IP):c.2219C>T (p.Pro740Leu)	not specified [RCV004866086]	uncertain significance	2	219611718	219611718	Human		name
597747554	CV3614824	single nucleotide variant	NM_052902.4(STK11IP):c.2527G>A (p.Gly843Arg)	not specified [RCV004866087]	uncertain significance	2	219613215	219613215	Human		name
598207352	CV3919651	single nucleotide variant	NM_052902.4(STK11IP):c.1279G>A (p.Gly427Ser)	not specified [RCV005291271]	uncertain significance	2	219608106	219608106	Human		name
598251448	CV3919652	single nucleotide variant	NM_052902.4(STK11IP):c.2597G>T (p.Gly866Val)	not specified [RCV005277890]	uncertain significance	2	219613811	219613811	Human		name
598251453	CV3919653	single nucleotide variant	NM_052902.4(STK11IP):c.1555G>A (p.Glu519Lys)	not specified [RCV005277891]	uncertain significance	2	219608382	219608382	Human		name
598207358	CV3919654	single nucleotide variant	NM_052902.4(STK11IP):c.2991G>T (p.Glu997Asp)	not specified [RCV005291272]	uncertain significance	2	219615215	219615215	Human		name
598207364	CV3919655	single nucleotide variant	NM_052902.4(STK11IP):c.2146G>A (p.Val716Ile)	not specified [RCV005291273]	uncertain significance	2	219611645	219611645	Human		name
598251459	CV3919657	single nucleotide variant	NM_052902.4(STK11IP):c.2241C>G (p.His747Gln)	not specified [RCV005277892]	uncertain significance	2	219611740	219611740	Human		name
598207375	CV3919658	single nucleotide variant	NM_052902.4(STK11IP):c.2675G>A (p.Arg892Gln)	not specified [RCV005291275]	uncertain significance	2	219613889	219613889	Human		name
598207381	CV3919659	single nucleotide variant	NM_052902.4(STK11IP):c.2855C>T (p.Ala952Val)	not specified [RCV005291276]	likely benign	2	219614532	219614532	Human		name
598207387	CV3919660	single nucleotide variant	NM_052902.4(STK11IP):c.1688C>T (p.Ser563Phe)	not specified [RCV005291277]	uncertain significance	2	219608667	219608667	Human		name
598207409	CV3919663	single nucleotide variant	NM_052902.4(STK11IP):c.2297C>G (p.Pro766Arg)	not specified [RCV005291280]	uncertain significance	2	219611796	219611796	Human		name
156075587	CV2350889	single nucleotide variant	NM_052902.4(STK11IP):c.3097C>T (p.Arg1033Trp)	not specified [RCV004211726]	uncertain significance	2	219615321	219615321	Human		name
155905028	CV2385660	single nucleotide variant	NM_052902.4(STK11IP):c.3005C>T (p.Ser1002Leu)	not specified [RCV004233291]	likely benign	2	219615229	219615229	Human		name
156221532	CV2394459	single nucleotide variant	NM_052902.4(STK11IP):c.3149G>A (p.Arg1050His)	not specified [RCV004240826]	uncertain significance	2	219616075	219616075	Human		name
401762824	CV2707254	single nucleotide variant	NM_052902.4(STK11IP):c.3091G>T (p.Asp1031Tyr)	not specified [RCV004310875]	uncertain significance	2	219615315	219615315	Human		name
405741540	CV3334444	single nucleotide variant	NM_052902.4(STK11IP):c.3025C>T (p.Arg1009Cys)	not specified [RCV004465657]	uncertain significance	2	219615249	219615249	Human		name
405741534	CV3334445	single nucleotide variant	NM_052902.4(STK11IP):c.3049A>G (p.Ser1017Gly)	not specified [RCV004465658]	uncertain significance	2	219615273	219615273	Human		name
405741527	CV3334446	single nucleotide variant	NM_052902.4(STK11IP):c.3080C>T (p.Ser1027Leu)	not specified [RCV004465659]	uncertain significance	2	219615304	219615304	Human		name
407496299	CV3485489	single nucleotide variant	NM_052902.4(STK11IP):c.3256C>A (p.Leu1086Ile)	not specified [RCV004668100]	uncertain significance	2	219616182	219616182	Human		name
597794461	CV3614808	single nucleotide variant	NM_052902.4(STK11IP):c.3235G>A (p.Val1079Met)	not specified [RCV004877860]	uncertain significance	2	219616161	219616161	Human		name
597747512	CV3614814	single nucleotide variant	NM_052902.4(STK11IP):c.3002C>T (p.Pro1001Leu)	not specified [RCV004866079]	uncertain significance	2	219615226	219615226	Human		name
598207369	CV3919656	single nucleotide variant	NM_052902.4(STK11IP):c.3230G>A (p.Arg1077Gln)	not specified [RCV005291274]	uncertain significance	2	219616156	219616156	Human		name

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