Baiap3 Variant Search Result - Rat Genome Database

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203 records found for search term Baiap3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597733043	CV3635022	single nucleotide variant	NM_001199097.2(BAIAP3):c.-6C>T	not specified [RCV004889114]	uncertain significance	16	1338544	1338544	Human		name
598275761	CV3933668	single nucleotide variant	NM_001199097.2(BAIAP3):c.-3G>A	not specified [RCV005304895]	likely benign	16	1338547	1338547	Human		name
156172869	CV2194299	single nucleotide variant	NM_001199097.2(BAIAP3):c.-11+985G>A	not specified [RCV004079416]	uncertain significance	16	1334734	1334734	Human		name
156057226	CV2396325	single nucleotide variant	NM_001199097.2(BAIAP3):c.-11+991G>A	not specified [RCV004242055]	uncertain significance	16	1334740	1334740	Human		name
329382567	CV2449148	single nucleotide variant	NM_001199097.2(BAIAP3):c.-11+926G>T	not specified [RCV004264206]	uncertain significance	16	1334675	1334675	Human		name
401744920	CV2698426	single nucleotide variant	NM_001199097.2(BAIAP3):c.-11+923G>A	not specified [RCV004298941]	likely benign	16	1334672	1334672	Human		name
401877044	CV2767806	single nucleotide variant	NM_001199097.2(BAIAP3):c.-11+996C>G	not specified [RCV004345928]	uncertain significance	16	1334745	1334745	Human		name
407453829	CV3416397	single nucleotide variant	NM_001199097.2(BAIAP3):c.-11+965T>C	not provided [RCV004597655]	benign	16	1334714	1334714	Human		name
597731741	CV3634928	single nucleotide variant	NM_001199097.2(BAIAP3):c.5C>T (p.Ser2Leu)	not specified [RCV004889020]	uncertain significance	16	1338554	1338554	Human		name
155914740	CV2264644	single nucleotide variant	NM_001199097.2(BAIAP3):c.26G>A (p.Ser9Asn)	not specified [RCV004132645]	uncertain significance	16	1338575	1338575	Human		name
156262913	CV2377065	single nucleotide variant	NM_001199097.2(BAIAP3):c.26G>C (p.Ser9Thr)	not specified [RCV004229740]	uncertain significance	16	1338575	1338575	Human		name
156004151	CV2396869	single nucleotide variant	NM_001199097.2(BAIAP3):c.31G>A (p.Val11Met)	not specified [RCV004233994]	uncertain significance	16	1338580	1338580	Human		name
401780276	CV2725968	single nucleotide variant	NM_001199097.2(BAIAP3):c.78G>T (p.Glu26Asp)	not specified [RCV004324335]	uncertain significance	16	1338627	1338627	Human		name
405265872	CV3220897	single nucleotide variant	NM_001199097.2(BAIAP3):c.891C>T (p.Asn297=)	BAIAP3-related disorder [RCV003969061]	likely benign	16	1342217	1342217	Human		name , trait , alternate_id
598182915	CV3933630	single nucleotide variant	NM_001199097.2(BAIAP3):c.65G>A (p.Arg22His)	not specified [RCV005311316]	uncertain significance	16	1338614	1338614	Human		name
156269673	CV2240179	single nucleotide variant	NM_001199097.2(BAIAP3):c.136C>G (p.Pro46Ala)	not specified [RCV004110937]	uncertain significance	16	1338906	1338906	Human		name
156114590	CV2264062	single nucleotide variant	NM_001199097.2(BAIAP3):c.265C>A (p.Pro89Thr)	not specified [RCV004138075]	uncertain significance	16	1339209	1339209	Human		name
156283510	CV2348944	single nucleotide variant	NM_001199097.2(BAIAP3):c.229C>T (p.Arg77Cys)	not specified [RCV004203377]	uncertain significance	16	1339173	1339173	Human		name
155933215	CV2399282	single nucleotide variant	NM_001199097.2(BAIAP3):c.118G>T (p.Ala40Ser)	not specified [RCV004242578]	uncertain significance	16	1338667	1338667	Human		name
329400283	CV2437570	single nucleotide variant	NM_001199097.2(BAIAP3):c.244G>T (p.Ala82Ser)	not specified [RCV004258853]	uncertain significance	16	1339188	1339188	Human		name
401720941	CV2673544	single nucleotide variant	NM_001199097.2(BAIAP3):c.188G>A (p.Gly63Glu)	not specified [RCV004288509]	uncertain significance	16	1338958	1338958	Human		name
401782064	CV2686511	single nucleotide variant	NM_001199097.2(BAIAP3):c.239C>T (p.Ser80Leu)	not specified [RCV004299953]	uncertain significance	16	1339183	1339183	Human		name
401870092	CV2772616	single nucleotide variant	NM_001199097.2(BAIAP3):c.220G>C (p.Val74Leu)	not specified [RCV004355367]	uncertain significance	16	1339164	1339164	Human		name
401904680	CV2810771	single nucleotide variant	NM_001199097.2(BAIAP3):c.122C>T (p.Thr41Met)	not provided [RCV003395168]	benign	16	1338671	1338671	Human		name
401904685	CV2810775	single nucleotide variant	NM_001199097.2(BAIAP3):c.2022C>T (p.Asp674=)	not provided [RCV003395172]	benign	16	1345330	1345330	Human		name
405691919	CV3290910	single nucleotide variant	NM_001199097.2(BAIAP3):c.148G>A (p.Val50Met)	not specified [RCV004423823]	uncertain significance	16	1338918	1338918	Human		name
407494304	CV3417356	single nucleotide variant	NM_001199097.2(BAIAP3):c.206T>C (p.Leu69Ser)	not specified [RCV004605559]	uncertain significance	16	1338976	1338976	Human		name
597730706	CV3634775	single nucleotide variant	NM_001199097.2(BAIAP3):c.230G>A (p.Arg77His)	not specified [RCV004888867]	uncertain significance	16	1339174	1339174	Human		name
597732463	CV3634969	single nucleotide variant	NM_001199097.2(BAIAP3):c.139G>A (p.Gly47Arg)	not specified [RCV004889061]	uncertain significance	16	1338909	1338909	Human		name
598241614	CV3933774	single nucleotide variant	NM_001199097.2(BAIAP3):c.1266G>A (p.Leu422=)	not specified [RCV005296961]	likely benign	16	1343393	1343393	Human		name
598241857	CV3933850	single nucleotide variant	NM_001199097.2(BAIAP3):c.212G>C (p.Cys71Ser)	not specified [RCV005297004]	uncertain significance	16	1338982	1338982	Human		name
8635671	CV90893	single nucleotide variant	NM_001199096.1(BAIAP3):c.1755G>A (p.Leu585=)	Malignant melanoma [RCV000070991]	not provided	16	1345022	1345022	Human		name
156318315	CV2200294	single nucleotide variant	NM_001199097.2(BAIAP3):c.386C>T (p.Ala129Val)	not specified [RCV004076631]	uncertain significance	16	1339581	1339581	Human		name
155929075	CV2224490	single nucleotide variant	NM_001199097.2(BAIAP3):c.883C>G (p.Arg295Gly)	not specified [RCV004098080]	uncertain significance	16	1342209	1342209	Human		name
155977365	CV2266404	single nucleotide variant	NM_001199097.2(BAIAP3):c.376G>A (p.Asp126Asn)	not specified [RCV004130999]	uncertain significance	16	1339571	1339571	Human		name
156006820	CV2288930	single nucleotide variant	NM_001199097.2(BAIAP3):c.590G>A (p.Arg197Gln)	not specified [RCV004149898]	uncertain significance	16	1341348	1341348	Human		name
155974409	CV2342549	single nucleotide variant	NM_001199097.2(BAIAP3):c.347C>T (p.Ala116Val)	not specified [RCV004196646]	uncertain significance	16	1339542	1339542	Human		name
156101224	CV2347779	single nucleotide variant	NM_001199097.2(BAIAP3):c.848T>G (p.Met283Arg)	not specified [RCV004195438]	uncertain significance	16	1342057	1342057	Human		name
156281304	CV2348535	single nucleotide variant	NM_001199097.2(BAIAP3):c.310C>T (p.Leu104Phe)	not specified [RCV004193718]	uncertain significance	16	1339505	1339505	Human		name
156116761	CV2349412	single nucleotide variant	NM_001199097.2(BAIAP3):c.646G>A (p.Gly216Ser)	not specified [RCV004199341]	likely benign	16	1341404	1341404	Human		name
156383160	CV2361435	single nucleotide variant	NM_001199097.2(BAIAP3):c.730T>C (p.Phe244Leu)	not specified [RCV004221079]	uncertain significance	16	1341488	1341488	Human		name
156072313	CV2376824	single nucleotide variant	NM_001199097.2(BAIAP3):c.369G>C (p.Gln123His)	not specified [RCV004227483]	uncertain significance	16	1339564	1339564	Human		name
156056929	CV2396293	single nucleotide variant	NM_001199097.2(BAIAP3):c.322G>A (p.Ala108Thr)	not specified [RCV004240237]	uncertain significance	16	1339517	1339517	Human		name
329367026	CV2442048	single nucleotide variant	NM_001199097.2(BAIAP3):c.503G>A (p.Arg168His)	not specified [RCV004262204]	uncertain significance	16	1341163	1341163	Human		name
329360730	CV2462904	single nucleotide variant	NM_001199097.2(BAIAP3):c.809C>T (p.Ala270Val)	not specified [RCV004272746]	uncertain significance	16	1342018	1342018	Human		name
401730053	CV2683925	single nucleotide variant	NM_001199097.2(BAIAP3):c.361C>G (p.Pro121Ala)	not specified [RCV004284645]	uncertain significance	16	1339556	1339556	Human		name
401733429	CV2685523	single nucleotide variant	NM_001199097.2(BAIAP3):c.692G>A (p.Ser231Asn)	not specified [RCV004294542]	uncertain significance	16	1341450	1341450	Human		name
401886890	CV2767950	single nucleotide variant	NM_001199097.2(BAIAP3):c.682G>A (p.Glu228Lys)	not specified [RCV004348200]	uncertain significance	16	1341440	1341440	Human		name
401904682	CV2810772	single nucleotide variant	NM_001199097.2(BAIAP3):c.893G>A (p.Gly298Glu)	not provided [RCV003395169]	likely benign	16	1342219	1342219	Human		name
405691789	CV3290888	single nucleotide variant	NM_001199097.2(BAIAP3):c.952G>A (p.Val318Ile)	not specified [RCV004423801]	likely benign	16	1342278	1342278	Human		name
405691795	CV3290889	single nucleotide variant	NM_001199097.2(BAIAP3):c.956G>A (p.Arg319Gln)	not specified [RCV004423802]	uncertain significance	16	1342282	1342282	Human		name
405691977	CV3290921	single nucleotide variant	NM_001199097.2(BAIAP3):c.309G>A (p.Met103Ile)	not specified [RCV004423834]	uncertain significance	16	1339504	1339504	Human		name
405691984	CV3290922	single nucleotide variant	NM_001199097.2(BAIAP3):c.310C>G (p.Leu104Val)	not specified [RCV004423835]	uncertain significance	16	1339505	1339505	Human		name
405691996	CV3290924	single nucleotide variant	NM_001199097.2(BAIAP3):c.727C>G (p.Leu243Val)	not specified [RCV004423837]	uncertain significance	16	1341485	1341485	Human		name
405692002	CV3290925	single nucleotide variant	NM_001199097.2(BAIAP3):c.855G>C (p.Arg285Ser)	not specified [RCV004423838]	uncertain significance	16	1342181	1342181	Human		name
407494271	CV3417348	single nucleotide variant	NM_001199097.2(BAIAP3):c.598C>T (p.Arg200Cys)	not specified [RCV004605552]	uncertain significance	16	1341356	1341356	Human		name
407494275	CV3417349	single nucleotide variant	NM_001199097.2(BAIAP3):c.616C>T (p.Arg206Cys)	not specified [RCV004605553]	uncertain significance	16	1341374	1341374	Human		name
597732124	CV3634888	single nucleotide variant	NM_001199097.2(BAIAP3):c.668G>C (p.Cys223Ser)	not specified [RCV004888980]	uncertain significance	16	1341426	1341426	Human		name
597731428	CV3634899	single nucleotide variant	NM_001199097.2(BAIAP3):c.922G>A (p.Asp308Asn)	not specified [RCV004888991]	uncertain significance	16	1342248	1342248	Human		name
597731509	CV3634907	single nucleotide variant	NM_001199097.2(BAIAP3):c.325C>G (p.Leu109Val)	not specified [RCV004888999]	uncertain significance	16	1339520	1339520	Human		name
598183058	CV3933688	single nucleotide variant	NM_001199097.2(BAIAP3):c.643C>T (p.Arg215Cys)	not specified [RCV005311340]	uncertain significance	16	1341401	1341401	Human		name
598275816	CV3933757	single nucleotide variant	NM_001199097.2(BAIAP3):c.616C>G (p.Arg206Gly)	not specified [RCV005304950]	uncertain significance	16	1341374	1341374	Human		name
598241798	CV3933830	single nucleotide variant	NM_001199097.2(BAIAP3):c.845G>T (p.Gly282Val)	not specified [RCV005296995]	uncertain significance	16	1342054	1342054	Human		name
598195726	CV3933841	single nucleotide variant	NM_001199097.2(BAIAP3):c.497T>A (p.Val166Asp)	not specified [RCV005313382]	uncertain significance	16	1341157	1341157	Human		name
10398629	CV204151	single nucleotide variant	NM_001199097.2(BAIAP3):c.2563G>C (p.Ala855Pro)	Long QT syndrome [RCV000190195]	likely benign	16	1346605	1346605	Human	2	name
156184491	CV2195492	single nucleotide variant	NM_001199097.2(BAIAP3):c.2093A>G (p.His698Arg)	not specified [RCV004082715]	uncertain significance	16	1345775	1345775	Human		name
156077474	CV2198235	single nucleotide variant	NM_001199097.2(BAIAP3):c.2332G>A (p.Val778Met)	not specified [RCV004079815]	uncertain significance	16	1346200	1346200	Human		name
156084991	CV2205630	single nucleotide variant	NM_001199097.2(BAIAP3):c.2296G>A (p.Glu766Lys)	not specified [RCV004082544]	uncertain significance	16	1346073	1346073	Human		name
156136940	CV2210335	single nucleotide variant	NM_001199097.2(BAIAP3):c.2618C>T (p.Ser873Leu)	not specified [RCV004089491]	uncertain significance	16	1346660	1346660	Human		name
155921002	CV2210947	single nucleotide variant	NM_001199097.2(BAIAP3):c.2900A>C (p.Lys967Thr)	not specified [RCV004086021]	uncertain significance	16	1347621	1347621	Human		name
155980113	CV2211890	single nucleotide variant	NM_001199097.2(BAIAP3):c.2848C>T (p.His950Tyr)	not specified [RCV004087023]	uncertain significance	16	1347569	1347569	Human		name
156401121	CV2213930	single nucleotide variant	NM_001199097.2(BAIAP3):c.2960C>T (p.Ala987Val)	not specified [RCV004083656]	uncertain significance	16	1347756	1347756	Human		name
156183087	CV2222355	single nucleotide variant	NM_001199097.2(BAIAP3):c.2083T>C (p.Ser695Pro)	not specified [RCV004099227]	uncertain significance	16	1345765	1345765	Human		name
155988451	CV2234211	single nucleotide variant	NM_001199097.2(BAIAP3):c.1496T>C (p.Leu499Pro)	not specified [RCV004106293]	uncertain significance	16	1344131	1344131	Human		name
155951170	CV2238740	single nucleotide variant	NM_001199097.2(BAIAP3):c.2320A>G (p.Asn774Asp)	not specified [RCV004107625]	likely benign	16	1346188	1346188	Human		name
156098427	CV2253267	single nucleotide variant	NM_001199097.2(BAIAP3):c.1312T>G (p.Tyr438Asp)	not specified [RCV004122803]	uncertain significance	16	1343439	1343439	Human		name
155993672	CV2253607	single nucleotide variant	NM_001199097.2(BAIAP3):c.1501C>A (p.Leu501Met)	not specified [RCV004125293]	uncertain significance	16	1344136	1344136	Human		name
156087833	CV2259009	single nucleotide variant	NM_001199097.2(BAIAP3):c.1510A>C (p.Lys504Gln)	not specified [RCV004120277]	uncertain significance	16	1344145	1344145	Human		name
156101895	CV2260376	single nucleotide variant	NM_001199097.2(BAIAP3):c.1733G>A (p.Ser578Asn)	not specified [RCV004129451]	uncertain significance	16	1344674	1344674	Human		name
156339043	CV2271362	single nucleotide variant	NM_001199097.2(BAIAP3):c.2911C>G (p.Leu971Val)	not specified [RCV004136475]	uncertain significance	16	1347707	1347707	Human		name
156169375	CV2276737	single nucleotide variant	NM_001199097.2(BAIAP3):c.1070A>G (p.Asp357Gly)	not specified [RCV004146523]	uncertain significance	16	1342723	1342723	Human		name
155903843	CV2298695	single nucleotide variant	NM_001199097.2(BAIAP3):c.2054A>G (p.Asp685Gly)	not specified [RCV004156270]	uncertain significance	16	1345362	1345362	Human		name
155905816	CV2303186	single nucleotide variant	NM_001199097.2(BAIAP3):c.2090G>C (p.Arg697Thr)	not specified [RCV004156949]	uncertain significance	16	1345772	1345772	Human		name
155951792	CV2309788	single nucleotide variant	NM_001199097.2(BAIAP3):c.1483G>A (p.Ala495Thr)	not specified [RCV004160908]	uncertain significance	16	1344118	1344118	Human		name
156253131	CV2311434	single nucleotide variant	NM_001199097.2(BAIAP3):c.1450C>T (p.Leu484Phe)	not specified [RCV004168280]	uncertain significance	16	1344085	1344085	Human		name
156335646	CV2333558	single nucleotide variant	NM_001199097.2(BAIAP3):c.2924G>A (p.Arg975Gln)	not specified [RCV004190244]	uncertain significance	16	1347720	1347720	Human		name
155971719	CV2335714	single nucleotide variant	NM_001199097.2(BAIAP3):c.1942G>A (p.Asp648Asn)	not specified [RCV004193915]	uncertain significance	16	1345250	1345250	Human		name
155921528	CV2340468	single nucleotide variant	NM_001199097.2(BAIAP3):c.1652G>A (p.Arg551Gln)	not specified [RCV004197195]	uncertain significance	16	1344518	1344518	Human		name
156041178	CV2342110	single nucleotide variant	NM_001199097.2(BAIAP3):c.2328G>C (p.Glu776Asp)	not specified [RCV004191705]	uncertain significance	16	1346196	1346196	Human		name
156134919	CV2362133	single nucleotide variant	NM_001199097.2(BAIAP3):c.2785G>A (p.Gly929Ser)	not specified [RCV004209937]	uncertain significance	16	1347331	1347331	Human		name
156052282	CV2363376	single nucleotide variant	NM_001199097.2(BAIAP3):c.2032T>C (p.Trp678Arg)	not specified [RCV004213914]	uncertain significance	16	1345340	1345340	Human		name
156099633	CV2367415	single nucleotide variant	NM_001199097.2(BAIAP3):c.2921A>G (p.Asn974Ser)	not specified [RCV004209314]	uncertain significance	16	1347717	1347717	Human		name
156004628	CV2396968	single nucleotide variant	NM_001199097.2(BAIAP3):c.1648C>T (p.Pro550Ser)	not specified [RCV004234078]	uncertain significance	16	1344514	1344514	Human		name
329361637	CV2437717	single nucleotide variant	NM_001199097.2(BAIAP3):c.2798A>G (p.Glu933Gly)	not specified [RCV004261028]	uncertain significance	16	1347344	1347344	Human		name
329364960	CV2439949	single nucleotide variant	NM_001199097.2(BAIAP3):c.2813G>C (p.Gly938Ala)	not specified [RCV004260430]	uncertain significance	16	1347359	1347359	Human		name
329391487	CV2448617	single nucleotide variant	NM_001199097.2(BAIAP3):c.1793G>A (p.Arg598Gln)	not specified [RCV004259289]	uncertain significance	16	1344833	1344833	Human		name
329378075	CV2459109	single nucleotide variant	NM_001199097.2(BAIAP3):c.2075T>G (p.Val692Gly)	not specified [RCV004272567]	uncertain significance	16	1345757	1345757	Human		name
329396372	CV2459601	single nucleotide variant	NM_001199097.2(BAIAP3):c.2864G>A (p.Arg955His)	not specified [RCV004277048]	uncertain significance	16	1347585	1347585	Human		name
329378732	CV2459918	single nucleotide variant	NM_001199097.2(BAIAP3):c.2773G>A (p.Ala925Thr)	not specified [RCV004279409]	uncertain significance	16	1347319	1347319	Human		name
329376101	CV2465201	single nucleotide variant	NM_001199097.2(BAIAP3):c.1013C>T (p.Ala338Val)	not specified [RCV004287237]	uncertain significance	16	1342582	1342582	Human		name
401722787	CV2677101	single nucleotide variant	NM_001199097.2(BAIAP3):c.1304C>T (p.Thr435Met)	not specified [RCV004295738]	uncertain significance	16	1343431	1343431	Human		name
401755470	CV2682494	single nucleotide variant	NM_001199097.2(BAIAP3):c.1988C>T (p.Pro663Leu)	not specified [RCV004290516]	uncertain significance	16	1345296	1345296	Human		name
401774519	CV2691765	single nucleotide variant	NM_001199097.2(BAIAP3):c.1240C>G (p.Leu414Val)	not specified [RCV004299219]	uncertain significance	16	1342991	1342991	Human		name
401745166	CV2698481	single nucleotide variant	NM_001199097.2(BAIAP3):c.1664G>A (p.Gly555Glu)	not specified [RCV004298985]	uncertain significance	16	1344605	1344605	Human		name
401740936	CV2702707	single nucleotide variant	NM_001199097.2(BAIAP3):c.2926T>C (p.Phe976Leu)	not specified [RCV004318960]	uncertain significance	16	1347722	1347722	Human		name
401741258	CV2713438	single nucleotide variant	NM_001199097.2(BAIAP3):c.2912T>G (p.Leu971Arg)	not specified [RCV004319054]	uncertain significance	16	1347708	1347708	Human		name
401725406	CV2721757	single nucleotide variant	NM_001199097.2(BAIAP3):c.1769T>C (p.Val590Ala)	not specified [RCV004324496]	uncertain significance	16	1344809	1344809	Human		name
401890171	CV2762342	single nucleotide variant	NM_001199097.2(BAIAP3):c.2863C>A (p.Arg955Ser)	not specified [RCV004335455]	uncertain significance	16	1347584	1347584	Human		name
401865968	CV2762473	single nucleotide variant	NM_001199097.2(BAIAP3):c.1976C>T (p.Ala659Val)	not specified [RCV004338010]	uncertain significance	16	1345284	1345284	Human		name
401870138	CV2765645	single nucleotide variant	NM_001199097.2(BAIAP3):c.2557G>A (p.Asp853Asn)	not specified [RCV004335657]	uncertain significance	16	1346505	1346505	Human		name
401904683	CV2810773	single nucleotide variant	NM_001199097.2(BAIAP3):c.1091G>C (p.Gly364Ala)	not provided [RCV003395170]	benign	16	1342744	1342744	Human		name
401904684	CV2810774	single nucleotide variant	NM_001199097.2(BAIAP3):c.1624G>A (p.Asp542Asn)	not provided [RCV003395171]	benign	16	1344490	1344490	Human		name
401930191	CV2810776	single nucleotide variant	NM_001199097.2(BAIAP3):c.2387C>T (p.Thr796Met)	not provided [RCV003390603]	benign	16	1346255	1346255	Human		name
405691807	CV3290891	single nucleotide variant	NM_001199097.2(BAIAP3):c.1010G>C (p.Ser337Thr)	not specified [RCV004423804]	uncertain significance	16	1342579	1342579	Human		name
405691812	CV3290892	single nucleotide variant	NM_001199097.2(BAIAP3):c.1082G>A (p.Ser361Asn)	not specified [RCV004423805]	uncertain significance	16	1342735	1342735	Human		name
405691822	CV3290893	single nucleotide variant	NM_001199097.2(BAIAP3):c.1285C>A (p.Arg429Ser)	not specified [RCV004423806]	uncertain significance	16	1343412	1343412	Human		name
405691826	CV3290894	single nucleotide variant	NM_001199097.2(BAIAP3):c.1489C>T (p.His497Tyr)	not specified [RCV004423807]	likely benign	16	1344124	1344124	Human		name
405691832	CV3290895	single nucleotide variant	NM_001199097.2(BAIAP3):c.1556G>A (p.Cys519Tyr)	not specified [RCV004423808]	uncertain significance	16	1344271	1344271	Human		name
405691841	CV3290896	single nucleotide variant	NM_001199097.2(BAIAP3):c.1580T>C (p.Met527Thr)	not specified [RCV004423809]	uncertain significance	16	1344295	1344295	Human		name
405691845	CV3290897	single nucleotide variant	NM_001199097.2(BAIAP3):c.1606G>A (p.Gly536Ser)	not specified [RCV004423810]	uncertain significance	16	1344472	1344472	Human		name
405691851	CV3290898	single nucleotide variant	NM_001199097.2(BAIAP3):c.1714G>A (p.Asp572Asn)	not specified [RCV004423811]	uncertain significance	16	1344655	1344655	Human		name
405691858	CV3290899	single nucleotide variant	NM_001199097.2(BAIAP3):c.1774G>A (p.Val592Ile)	not specified [RCV004423812]	uncertain significance	16	1344814	1344814	Human		name
405691871	CV3290901	single nucleotide variant	NM_001199097.2(BAIAP3):c.1805G>A (p.Arg602His)	not specified [RCV004423814]	uncertain significance	16	1344845	1344845	Human		name
405691878	CV3290902	single nucleotide variant	NM_001199097.2(BAIAP3):c.1885G>C (p.Glu629Gln)	not specified [RCV004423815]	uncertain significance	16	1345044	1345044	Human		name
405691882	CV3290903	single nucleotide variant	NM_001199097.2(BAIAP3):c.2063C>T (p.Thr688Met)	not specified [RCV004423816]	uncertain significance	16	1345371	1345371	Human		name
405691888	CV3290904	single nucleotide variant	NM_001199097.2(BAIAP3):c.2074G>C (p.Val692Leu)	not specified [RCV004423817]	uncertain significance	16	1345756	1345756	Human		name
405691895	CV3290905	single nucleotide variant	NM_001199097.2(BAIAP3):c.2213T>C (p.Val738Ala)	not specified [RCV004423818]	uncertain significance	16	1345990	1345990	Human		name
405691900	CV3290906	single nucleotide variant	NM_001199097.2(BAIAP3):c.2245C>T (p.Leu749Phe)	not specified [RCV004423819]	uncertain significance	16	1346022	1346022	Human		name
405691904	CV3290907	single nucleotide variant	NM_001199097.2(BAIAP3):c.2248C>T (p.Arg750Trp)	not specified [RCV004423820]	uncertain significance	16	1346025	1346025	Human		name
405691909	CV3290908	single nucleotide variant	NM_001199097.2(BAIAP3):c.2363G>C (p.Gly788Ala)	not specified [RCV004423821]	uncertain significance	16	1346231	1346231	Human		name
405691915	CV3290909	single nucleotide variant	NM_001199097.2(BAIAP3):c.2410C>T (p.Arg804Cys)	not specified [RCV004423822]	uncertain significance	16	1346278	1346278	Human		name
405691925	CV3290911	single nucleotide variant	NM_001199097.2(BAIAP3):c.2654C>T (p.Ala885Val)	not specified [RCV004423824]	uncertain significance	16	1346858	1346858	Human		name
405691935	CV3290913	single nucleotide variant	NM_001199097.2(BAIAP3):c.2945G>A (p.Arg982His)	not specified [RCV004423826]	uncertain significance	16	1347741	1347741	Human		name
405691940	CV3290914	single nucleotide variant	NM_001199097.2(BAIAP3):c.2980G>A (p.Val994Met)	not specified [RCV004423827]	uncertain significance	16	1347776	1347776	Human		name
407494279	CV3417350	single nucleotide variant	NM_001199097.2(BAIAP3):c.1823C>T (p.Ala608Val)	not specified [RCV004605554]	uncertain significance	16	1344982	1344982	Human		name
407494285	CV3417351	single nucleotide variant	NM_001199097.2(BAIAP3):c.2070G>C (p.Glu690Asp)	not specified [RCV004605555]	uncertain significance	16	1345752	1345752	Human		name
407494291	CV3417352	single nucleotide variant	NM_001199097.2(BAIAP3):c.2026G>A (p.Ala676Thr)	not specified [RCV004605556]	likely benign	16	1345334	1345334	Human		name
407494296	CV3417353	single nucleotide variant	NM_001199097.2(BAIAP3):c.1090G>A (p.Gly364Arg)	not specified [RCV004605557]	uncertain significance	16	1342743	1342743	Human		name
407494300	CV3417354	single nucleotide variant	NM_001199097.2(BAIAP3):c.2944C>T (p.Arg982Cys)	not specified [RCV004605558]	uncertain significance	16	1347740	1347740	Human		name
407494308	CV3417357	single nucleotide variant	NM_001199097.2(BAIAP3):c.2090G>A (p.Arg697Lys)	not specified [RCV004605560]	likely benign	16	1345772	1345772	Human		name
407499822	CV3417358	single nucleotide variant	NM_001199097.2(BAIAP3):c.2215T>G (p.Cys739Gly)	not specified [RCV004606969]	uncertain significance	16	1345992	1345992	Human		name
407494312	CV3417359	single nucleotide variant	NM_001199097.2(BAIAP3):c.2084C>T (p.Ser695Phe)	not specified [RCV004605561]	uncertain significance	16	1345766	1345766	Human		name
407494316	CV3417360	single nucleotide variant	NM_001199097.2(BAIAP3):c.1472C>T (p.Thr491Ile)	not specified [RCV004605562]	uncertain significance	16	1344107	1344107	Human		name
597730385	CV3634795	single nucleotide variant	NM_001199097.2(BAIAP3):c.2293A>G (p.Ser765Gly)	not specified [RCV004888887]	uncertain significance	16	1346070	1346070	Human		name
597730483	CV3634805	single nucleotide variant	NM_001199097.2(BAIAP3):c.1428C>G (p.Phe476Leu)	not specified [RCV004888897]	uncertain significance	16	1344063	1344063	Human		name
597730595	CV3634816	single nucleotide variant	NM_001199097.2(BAIAP3):c.2615C>T (p.Ala872Val)	not specified [RCV004888908]	uncertain significance	16	1346657	1346657	Human		name
597730616	CV3634818	single nucleotide variant	NM_001199097.2(BAIAP3):c.2036G>T (p.Arg679Met)	not specified [RCV004888910]	uncertain significance	16	1345344	1345344	Human		name
597730944	CV3634825	single nucleotide variant	NM_001199097.2(BAIAP3):c.2689G>A (p.Ala897Thr)	not specified [RCV004888917]	uncertain significance	16	1346893	1346893	Human		name
597731059	CV3634836	single nucleotide variant	NM_001199097.2(BAIAP3):c.1853A>G (p.Lys618Arg)	not specified [RCV004888928]	uncertain significance	16	1345012	1345012	Human		name
597732249	CV3634877	single nucleotide variant	NM_001199097.2(BAIAP3):c.1867G>A (p.Val623Met)	not specified [RCV004888969]	uncertain significance	16	1345026	1345026	Human		name
597731622	CV3634917	single nucleotide variant	NM_001199097.2(BAIAP3):c.2426G>C (p.Cys809Ser)	not specified [RCV004889009]	uncertain significance	16	1346294	1346294	Human		name
597731860	CV3634939	single nucleotide variant	NM_001199097.2(BAIAP3):c.2399G>T (p.Gly800Val)	not specified [RCV004889031]	uncertain significance	16	1346267	1346267	Human		name
597732343	CV3634958	single nucleotide variant	NM_001199097.2(BAIAP3):c.1920C>G (p.Phe640Leu)	not specified [RCV004889050]	uncertain significance	16	1345079	1345079	Human		name
597732594	CV3634980	single nucleotide variant	NM_001199097.2(BAIAP3):c.2050G>A (p.Val684Met)	not specified [RCV004889072]	uncertain significance	16	1345358	1345358	Human		name
597732706	CV3634990	single nucleotide variant	NM_001199097.2(BAIAP3):c.1963G>A (p.Ala655Thr)	not specified [RCV004889082]	uncertain significance	16	1345271	1345271	Human		name
597732917	CV3635011	single nucleotide variant	NM_001199097.2(BAIAP3):c.1075G>T (p.Ala359Ser)	not specified [RCV004889103]	uncertain significance	16	1342728	1342728	Human		name
597733166	CV3635034	single nucleotide variant	NM_001199097.2(BAIAP3):c.1709A>G (p.Tyr570Cys)	not specified [RCV004889126]	uncertain significance	16	1344650	1344650	Human		name
598275744	CV3933639	single nucleotide variant	NM_001199097.2(BAIAP3):c.2272G>A (p.Gly758Arg)	not specified [RCV005304878]	uncertain significance	16	1346049	1346049	Human		name
598183101	CV3933707	single nucleotide variant	NM_001199097.2(BAIAP3):c.2666T>A (p.Leu889Gln)	not specified [RCV005311347]	uncertain significance	16	1346870	1346870	Human		name
598183147	CV3933718	single nucleotide variant	NM_001199097.2(BAIAP3):c.2705G>A (p.Arg902His)	not specified [RCV005311354]	uncertain significance	16	1346909	1346909	Human		name
598275797	CV3933726	single nucleotide variant	NM_001199097.2(BAIAP3):c.1469C>A (p.Ala490Asp)	not specified [RCV005304931]	uncertain significance	16	1344104	1344104	Human		name
598275804	CV3933738	single nucleotide variant	NM_001199097.2(BAIAP3):c.2458G>C (p.Glu820Gln)	not specified [RCV005304938]	uncertain significance	16	1346326	1346326	Human		name
598275809	CV3933746	single nucleotide variant	NM_001199097.2(BAIAP3):c.1300T>C (p.Cys434Arg)	not specified [RCV005304943]	likely benign	16	1343427	1343427	Human		name
598183235	CV3933766	single nucleotide variant	NM_001199097.2(BAIAP3):c.1414G>A (p.Ala472Thr)	not specified [RCV005311369]	uncertain significance	16	1344049	1344049	Human		name
598183260	CV3933771	single nucleotide variant	NM_001199097.2(BAIAP3):c.2778G>C (p.Glu926Asp)	not specified [RCV005311373]	uncertain significance	16	1347324	1347324	Human		name
598195604	CV3933784	single nucleotide variant	NM_001199097.2(BAIAP3):c.1235G>A (p.Ser412Asn)	not specified [RCV005313357]	uncertain significance	16	1342986	1342986	Human		name
598241686	CV3933793	single nucleotide variant	NM_001199097.2(BAIAP3):c.2575C>T (p.Leu859Phe)	not specified [RCV005296974]	uncertain significance	16	1346617	1346617	Human		name
598195633	CV3933800	single nucleotide variant	NM_001199097.2(BAIAP3):c.2672T>C (p.Leu891Pro)	not specified [RCV005313364]	uncertain significance	16	1346876	1346876	Human		name
598241745	CV3933810	single nucleotide variant	NM_001199097.2(BAIAP3):c.2414C>G (p.Pro805Arg)	not specified [RCV005296985]	uncertain significance	16	1346282	1346282	Human		name
598195667	CV3933820	single nucleotide variant	NM_001199097.2(BAIAP3):c.2460G>C (p.Glu820Asp)	not specified [RCV005313371]	uncertain significance	16	1346328	1346328	Human		name
156368504	CV2197587	single nucleotide variant	NM_001199097.2(BAIAP3):c.3065C>T (p.Pro1022Leu)	not specified [RCV004074465]	uncertain significance	16	1347933	1347933	Human		name
156179730	CV2201681	single nucleotide variant	NM_001199097.2(BAIAP3):c.3241G>A (p.Gly1081Arg)	not specified [RCV004082135]	uncertain significance	16	1348187	1348187	Human		name
156401177	CV2210593	single nucleotide variant	NM_001199097.2(BAIAP3):c.3175C>T (p.Arg1059Cys)	not specified [RCV004083744]	uncertain significance	16	1348121	1348121	Human		name
156339049	CV2271363	single nucleotide variant	NM_001199097.2(BAIAP3):c.3268G>A (p.Val1090Ile)	not specified [RCV004136476]	likely benign	16	1348214	1348214	Human		name
156169140	CV2317060	single nucleotide variant	NM_001199097.2(BAIAP3):c.3094A>G (p.Arg1032Gly)	not specified [RCV004174549]	uncertain significance	16	1347962	1347962	Human		name
156052212	CV2320285	single nucleotide variant	NM_001199097.2(BAIAP3):c.3239C>T (p.Ala1080Val)	not specified [RCV004178453]	uncertain significance	16	1348185	1348185	Human		name
156053712	CV2329113	single nucleotide variant	NM_001199097.2(BAIAP3):c.3231C>A (p.Asn1077Lys)	not specified [RCV004173877]	uncertain significance	16	1348177	1348177	Human		name
156081723	CV2333845	single nucleotide variant	NM_001199097.2(BAIAP3):c.3173G>A (p.Arg1058His)	not specified [RCV004181344]	uncertain significance	16	1348119	1348119	Human		name
156283776	CV2334706	single nucleotide variant	NM_001199097.2(BAIAP3):c.3283C>T (p.Arg1095Trp)	not specified [RCV004188688]	uncertain significance	16	1348229	1348229	Human		name
156082340	CV2384846	single nucleotide variant	NM_001199097.2(BAIAP3):c.3291G>C (p.Gln1097His)	not specified [RCV004225728]	uncertain significance	16	1348237	1348237	Human		name
156089370	CV2392062	single nucleotide variant	NM_001199097.2(BAIAP3):c.3112C>T (p.Arg1038Trp)	not specified [RCV004237957]	uncertain significance	16	1347980	1347980	Human		name
329367381	CV2456787	single nucleotide variant	NM_001199097.2(BAIAP3):c.3229A>G (p.Asn1077Asp)	not specified [RCV004270760]	uncertain significance	16	1348175	1348175	Human		name
401765686	CV2683389	single nucleotide variant	NM_001199097.2(BAIAP3):c.3113G>A (p.Arg1038Gln)	not specified [RCV004288160]	uncertain significance	16	1347981	1347981	Human		name
401780793	CV2685723	single nucleotide variant	NM_001199097.2(BAIAP3):c.3163G>A (p.Glu1055Lys)	not specified [RCV004296769]	uncertain significance	16	1348109	1348109	Human		name
401769408	CV2689710	single nucleotide variant	NM_001199097.2(BAIAP3):c.3182C>T (p.Ala1061Val)	not specified [RCV004297627]	uncertain significance	16	1348128	1348128	Human		name
401782636	CV2697133	single nucleotide variant	NM_001199097.2(BAIAP3):c.3385C>T (p.Arg1129Cys)	not specified [RCV004302128]	uncertain significance	16	1348408	1348408	Human		name
401881454	CV2783840	single nucleotide variant	NM_001199097.2(BAIAP3):c.3242G>A (p.Gly1081Glu)	not specified [RCV004360743]	uncertain significance	16	1348188	1348188	Human		name
405691946	CV3290915	single nucleotide variant	NM_001199097.2(BAIAP3):c.3016G>C (p.Asp1006His)	not specified [RCV004423828]	uncertain significance	16	1347812	1347812	Human		name
405691952	CV3290916	single nucleotide variant	NM_001199097.2(BAIAP3):c.3167C>T (p.Ala1056Val)	not specified [RCV004423829]	uncertain significance	16	1348113	1348113	Human		name
405691958	CV3290917	single nucleotide variant	NM_001199097.2(BAIAP3):c.3178C>T (p.Arg1060Cys)	not specified [RCV004423830]	uncertain significance	16	1348124	1348124	Human		name
405691963	CV3290918	single nucleotide variant	NM_001199097.2(BAIAP3):c.3205A>G (p.Met1069Val)	not specified [RCV004423831]	uncertain significance	16	1348151	1348151	Human		name
405691967	CV3290919	single nucleotide variant	NM_001199097.2(BAIAP3):c.3280G>A (p.Ala1094Thr)	not specified [RCV004423832]	uncertain significance	16	1348226	1348226	Human		name
405691971	CV3290920	single nucleotide variant	NM_001199097.2(BAIAP3):c.3340C>T (p.Arg1114Trp)	not specified [RCV004423833]	uncertain significance	16	1348286	1348286	Human		name
407494266	CV3417347	single nucleotide variant	NM_001199097.2(BAIAP3):c.3284G>A (p.Arg1095Gln)	not specified [RCV004605551]	uncertain significance	16	1348230	1348230	Human		name
597730278	CV3634784	single nucleotide variant	NM_001199097.2(BAIAP3):c.3136G>A (p.Glu1046Lys)	not specified [RCV004888876]	uncertain significance	16	1348004	1348004	Human		name
597731146	CV3634846	single nucleotide variant	NM_001199097.2(BAIAP3):c.3085C>T (p.Arg1029Cys)	not specified [RCV004888938]	uncertain significance	16	1347953	1347953	Human		name
597731340	CV3634866	single nucleotide variant	NM_001199097.2(BAIAP3):c.3404A>C (p.Gln1135Pro)	not specified [RCV004888958]	uncertain significance	16	1348427	1348427	Human		name
597731961	CV3634948	single nucleotide variant	NM_001199097.2(BAIAP3):c.3088A>G (p.Ser1030Gly)	not specified [RCV004889040]	uncertain significance	16	1347956	1347956	Human		name
597732817	CV3635001	single nucleotide variant	NM_001199097.2(BAIAP3):c.3433G>A (p.Glu1145Lys)	not specified [RCV004889093]	uncertain significance	16	1348456	1348456	Human		name
597733273	CV3635044	single nucleotide variant	NM_001199097.2(BAIAP3):c.3269T>C (p.Val1090Ala)	not specified [RCV004889136]	uncertain significance	16	1348215	1348215	Human		name
597705724	CV3635053	single nucleotide variant	NM_001199097.2(BAIAP3):c.3049G>A (p.Val1017Met)	not specified [RCV004886169]	uncertain significance	16	1347917	1347917	Human		name
598183088	CV3933699	single nucleotide variant	NM_001199097.2(BAIAP3):c.3424A>C (p.Lys1142Gln)	not specified [RCV005311345]	uncertain significance	16	1348447	1348447	Human		name
598195764	CV3933858	single nucleotide variant	NM_001199097.2(BAIAP3):c.3425A>G (p.Lys1142Arg)	not specified [RCV005313390]	likely benign	16	1348448	1348448	Human		name

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