Afap1l2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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92 records found for search term Afap1l2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597642361	CV3663485	single nucleotide variant	NM_001001936.3(AFAP1L2):c.20T>C (p.Leu7Pro)	not specified [RCV004909335]	uncertain significance	10	114340728	114340728	Human		name
156233993	CV2197165	single nucleotide variant	NM_001001936.3(AFAP1L2):c.112G>A (p.Ala38Thr)	not specified [RCV004071586]	uncertain significance	10	114340636	114340636	Human		name
155948496	CV2245938	single nucleotide variant	NM_001001936.3(AFAP1L2):c.277C>T (p.Pro93Ser)	not specified [RCV004113563]	uncertain significance	10	114331841	114331841	Human		name
156250624	CV2359144	single nucleotide variant	NM_001001936.3(AFAP1L2):c.178G>A (p.Val60Met)	not specified [RCV004214502]	uncertain significance	10	114333263	114333263	Human		name
329382506	CV2424409	single nucleotide variant	NM_001001936.3(AFAP1L2):c.124C>T (p.Arg42Trp)	not specified [RCV004252305]	uncertain significance	10	114340624	114340624	Human		name
401907793	CV2809648	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2286C>T (p.His762=)	not provided [RCV003422909]	likely benign	10	114297241	114297241	Human		name
401907794	CV2809649	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1905C>G (p.Thr635=)	not provided [RCV003422910]	likely benign	10	114300246	114300246	Human		name
401907796	CV2809650	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1056G>A (p.Arg352=)	not provided [RCV003422911]	likely benign	10	114307821	114307821	Human		name
405727395	CV3259905	single nucleotide variant	NM_001001936.3(AFAP1L2):c.125G>A (p.Arg42Gln)	not specified [RCV004378786]	uncertain significance	10	114340623	114340623	Human		name
405727738	CV3259920	single nucleotide variant	NM_001001936.3(AFAP1L2):c.156G>C (p.Glu52Asp)	not specified [RCV004378801]	uncertain significance	10	114333285	114333285	Human		name
405728092	CV3259959	single nucleotide variant	NM_001001936.3(AFAP1L2):c.217A>G (p.Lys73Glu)	not specified [RCV004378840]	uncertain significance	10	114333224	114333224	Human		name
405743707	CV3260010	single nucleotide variant	NM_001001936.3(AFAP1L2):c.292C>G (p.Pro98Ala)	not specified [RCV004380965]	uncertain significance	10	114331826	114331826	Human		name
597642272	CV3663422	single nucleotide variant	NM_001001936.3(AFAP1L2):c.272C>T (p.Ser91Leu)	not specified [RCV004909320]	uncertain significance	10	114331846	114331846	Human		name
15186525	CV701192	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2190C>T (p.Arg730=)	not provided [RCV000953309]	benign\|likely benign	10	114297337	114297337	Human		name
15183394	CV723787	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1590G>A (p.Glu530=)	not provided [RCV000886216]	benign	10	114300643	114300643	Human		name
156270857	CV2195195	single nucleotide variant	NM_001001936.3(AFAP1L2):c.886G>A (p.Asp296Asn)	not specified [RCV004080137]	uncertain significance	10	114308514	114308514	Human		name
155931210	CV2220995	single nucleotide variant	NM_001001936.3(AFAP1L2):c.489G>T (p.Trp163Cys)	not specified [RCV004092679]	uncertain significance	10	114315683	114315683	Human		name
156241673	CV2265802	single nucleotide variant	NM_001001936.3(AFAP1L2):c.890T>C (p.Ile297Thr)	not specified [RCV004126418]	uncertain significance	10	114308510	114308510	Human		name
156029334	CV2278617	single nucleotide variant	NM_001001936.3(AFAP1L2):c.326G>A (p.Arg109Gln)	not specified [RCV004134830]	uncertain significance	10	114323251	114323251	Human		name
155940791	CV2294141	single nucleotide variant	NM_001001936.3(AFAP1L2):c.731T>C (p.Met244Thr)	not specified [RCV004149510]	uncertain significance	10	114313932	114313932	Human		name
156207144	CV2307874	single nucleotide variant	NM_001001936.3(AFAP1L2):c.382G>A (p.Glu128Lys)	not specified [RCV004170334]	uncertain significance	10	114323195	114323195	Human		name
156202584	CV2334726	single nucleotide variant	NM_001001936.3(AFAP1L2):c.526G>A (p.Ala176Thr)	not specified [RCV004188705]	uncertain significance	10	114315646	114315646	Human		name
155908405	CV2387313	single nucleotide variant	NM_001001936.3(AFAP1L2):c.454G>A (p.Asp152Asn)	not specified [RCV004238401]	uncertain significance	10	114315718	114315718	Human		name
156256228	CV2397745	single nucleotide variant	NM_001001936.3(AFAP1L2):c.529C>T (p.Arg177Cys)	not specified [RCV004239223]	uncertain significance	10	114315643	114315643	Human		name
329375467	CV2468627	single nucleotide variant	NM_001001936.3(AFAP1L2):c.958A>G (p.Thr320Ala)	not specified [RCV004278182]	uncertain significance	10	114308442	114308442	Human		name
329353161	CV2471510	single nucleotide variant	NM_001001936.3(AFAP1L2):c.392A>G (p.Asp131Gly)	not specified [RCV004280502]	uncertain significance	10	114323185	114323185	Human		name
401760751	CV2715921	single nucleotide variant	NM_001001936.3(AFAP1L2):c.830C>T (p.Ala277Val)	not specified [RCV004329027]	uncertain significance	10	114310406	114310406	Human		name
401871063	CV2766759	single nucleotide variant	NM_001001936.3(AFAP1L2):c.475G>A (p.Ala159Thr)	not specified [RCV004349149]	uncertain significance	10	114315697	114315697	Human		name
401862430	CV2775297	single nucleotide variant	NM_001001936.3(AFAP1L2):c.530G>A (p.Arg177His)	not specified [RCV004348414]	uncertain significance	10	114315642	114315642	Human		name
405743831	CV3260028	single nucleotide variant	NM_001001936.3(AFAP1L2):c.457G>A (p.Gly153Ser)	not specified [RCV004380983]	likely benign	10	114315715	114315715	Human		name
405744143	CV3260051	single nucleotide variant	NM_001001936.3(AFAP1L2):c.538G>A (p.Ala180Thr)	not specified [RCV004381006]	uncertain significance	10	114315634	114315634	Human		name
405744240	CV3260065	single nucleotide variant	NM_001001936.3(AFAP1L2):c.866G>A (p.Arg289His)	not specified [RCV004381020]	uncertain significance	10	114310370	114310370	Human		name
407478081	CV3431378	single nucleotide variant	NM_001001936.3(AFAP1L2):c.346A>G (p.Lys116Glu)	not specified [RCV004617448]	uncertain significance	10	114323231	114323231	Human		name
597642344	CV3663452	single nucleotide variant	NM_001001936.3(AFAP1L2):c.514C>G (p.Leu172Val)	not specified [RCV004909332]	uncertain significance	10	114315658	114315658	Human		name
597642356	CV3663469	single nucleotide variant	NM_001001936.3(AFAP1L2):c.694G>A (p.Val232Met)	not specified [RCV004909334]	uncertain significance	10	114313969	114313969	Human		name
598171558	CV3953195	single nucleotide variant	NM_001001936.3(AFAP1L2):c.318T>G (p.Ile106Met)	not specified [RCV005331204]	uncertain significance	10	114323259	114323259	Human		name
598171596	CV3953202	single nucleotide variant	NM_001001936.3(AFAP1L2):c.535T>C (p.Cys179Arg)	not specified [RCV005331211]	uncertain significance	10	114315637	114315637	Human		name
8633500	CV88715	single nucleotide variant	NM_001001936.3(AFAP1L2):c.490C>T (p.Pro164Ser)	not specified [RCV004092680]	uncertain significance\|not provided	10	114315682	114315682	Human		name
155963848	CV2194156	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1297G>A (p.Glu433Lys)	not specified [RCV004077246]	uncertain significance	10	114302472	114302472	Human		name
155960883	CV2204383	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2176G>A (p.Glu726Lys)	not specified [RCV004079200]	uncertain significance	10	114297351	114297351	Human		name
156329243	CV2216363	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2338G>T (p.Asp780Tyr)	not specified [RCV004097231]	uncertain significance	10	114297070	114297070	Human		name
155967991	CV2216949	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1387G>A (p.Asp463Asn)	not specified [RCV004085320]	uncertain significance	10	114302382	114302382	Human		name
156289498	CV2229918	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2447G>A (p.Gly816Glu)	not specified [RCV004105464]	uncertain significance	10	114296052	114296052	Human		name
156138555	CV2236706	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1487A>T (p.Gln496Leu)	not specified [RCV004110661]	uncertain significance	10	114301409	114301409	Human		name
155962781	CV2285695	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2252C>T (p.Pro751Leu)	not specified [RCV004141543]	uncertain significance	10	114297275	114297275	Human		name
156092001	CV2300103	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2387C>T (p.Ser796Leu)	not specified [RCV004151301]	uncertain significance	10	114297021	114297021	Human		name
155967640	CV2329944	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1655G>A (p.Ser552Asn)	not specified [RCV004183398]	uncertain significance	10	114300578	114300578	Human		name
156082229	CV2333957	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1627G>A (p.Val543Ile)	not specified [RCV004183489]	uncertain significance	10	114300606	114300606	Human		name
156135036	CV2347176	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2129C>T (p.Ala710Val)	not specified [RCV004204650]	uncertain significance	10	114297398	114297398	Human		name
156077396	CV2351032	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1943G>A (p.Arg648His)	not provided [RCV004695682]\|not specified [RCV004211856]	uncertain significance	10	114300208	114300208	Human		name
156082202	CV2368885	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1063G>A (p.Glu355Lys)	not specified [RCV004207842]	uncertain significance	10	114307814	114307814	Human		name
155991599	CV2384301	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1493G>A (p.Arg498His)	not specified [RCV004227685]	uncertain significance	10	114301403	114301403	Human		name
156053018	CV2385427	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1492C>T (p.Arg498Cys)	not specified [RCV004233081]	uncertain significance	10	114301404	114301404	Human		name
156152344	CV2394849	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2161G>A (p.Glu721Lys)	not specified [RCV004234509]	uncertain significance	10	114297366	114297366	Human		name
329381844	CV2424239	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1682C>G (p.Thr561Arg)	not specified [RCV004250360]	uncertain significance	10	114300551	114300551	Human		name
329360572	CV2439509	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1795G>A (p.Glu599Lys)	not specified [RCV004262448]	uncertain significance	10	114300356	114300356	Human		name
329387839	CV2440155	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2284C>A (p.His762Asn)	not specified [RCV004260611]	uncertain significance	10	114297243	114297243	Human		name
401766462	CV2679700	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2237A>G (p.Lys746Arg)	not specified [RCV004282170]	uncertain significance	10	114297290	114297290	Human		name
401744266	CV2680928	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1837G>A (p.Val613Ile)	not specified [RCV004296000]	uncertain significance	10	114300314	114300314	Human		name
401755398	CV2682472	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1678C>T (p.Pro560Ser)	not specified [RCV004290497]	uncertain significance	10	114300555	114300555	Human		name
401773365	CV2698187	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1481C>T (p.Pro494Leu)	not specified [RCV004304756]	uncertain significance	10	114301415	114301415	Human		name
401747947	CV2698892	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1005C>A (p.Asn335Lys)	not specified [RCV004301649]	uncertain significance	10	114307872	114307872	Human		name
401763039	CV2707456	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2238G>C (p.Lys746Asn)	not specified [RCV004312837]	uncertain significance	10	114297289	114297289	Human		name
401757907	CV2731531	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2372A>G (p.Lys791Arg)	not specified [RCV004330880]	uncertain significance	10	114297036	114297036	Human		name
401894719	CV2785224	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2269A>G (p.Thr757Ala)	not specified [RCV004356998]	uncertain significance	10	114297258	114297258	Human		name
401876981	CV2793305	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2138A>G (p.Glu713Gly)	not specified [RCV004362125]	uncertain significance	10	114297389	114297389	Human		name
401882189	CV2793398	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1156C>T (p.Arg386Trp)	not specified [RCV004362497]	uncertain significance	10	114304847	114304847	Human		name
405727192	CV3259881	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1010T>A (p.Met337Lys)	not specified [RCV004378762]	uncertain significance	10	114307867	114307867	Human		name
405727289	CV3259893	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1195G>A (p.Val399Met)	not specified [RCV004378774]	uncertain significance	10	114304808	114304808	Human		name
405727334	CV3259898	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1206G>T (p.Glu402Asp)	not specified [RCV004378779]	uncertain significance	10	114304797	114304797	Human		name
405727669	CV3259912	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1446G>T (p.Lys482Asn)	not specified [RCV004378793]	uncertain significance	10	114301450	114301450	Human		name
405727747	CV3259921	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1586A>C (p.Asn529Thr)	not specified [RCV004378802]	uncertain significance	10	114300647	114300647	Human		name
405728055	CV3259954	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2170C>T (p.Arg724Trp)	not specified [RCV004378835]	uncertain significance	10	114297357	114297357	Human		name
405743919	CV3259964	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2188C>T (p.Arg730Cys)	not specified [RCV004380919]	uncertain significance	10	114297339	114297339	Human		name
405743612	CV3259996	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2392G>A (p.Val798Met)	not specified [RCV004380951]	likely benign	10	114297016	114297016	Human		name
407478031	CV3431367	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1129G>A (p.Asp377Asn)	not specified [RCV004617437]	uncertain significance	10	114304874	114304874	Human		name
407478127	CV3441410	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1123G>C (p.Val375Leu)	not specified [RCV004617458]	uncertain significance	10	114304880	114304880	Human		name
597642213	CV3663411	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1412C>A (p.Ala471Glu)	not specified [RCV004909310]	uncertain significance	10	114302357	114302357	Human		name
597642317	CV3663431	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1426C>A (p.Leu476Ile)	not specified [RCV004909328]	uncertain significance	10	114302343	114302343	Human		name
597642323	CV3663433	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1894G>A (p.Val632Met)	not specified [RCV004909329]	uncertain significance	10	114300257	114300257	Human		name
597713191	CV3663440	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1925C>T (p.Pro642Leu)	not specified [RCV004918008]	uncertain significance	10	114300226	114300226	Human		name
597642335	CV3663445	single nucleotide variant	NM_001001936.3(AFAP1L2):c.2313A>C (p.Lys771Asn)	not specified [RCV004909331]	uncertain significance	10	114297095	114297095	Human		name
597642350	CV3663461	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1259A>G (p.Lys420Arg)	not specified [RCV004909333]	uncertain significance	10	114304744	114304744	Human		name
597713204	CV3663477	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1111C>T (p.Arg371Cys)	not specified [RCV004918009]	uncertain significance	10	114304892	114304892	Human		name
597713215	CV3663492	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1826G>C (p.Arg609Thr)	not specified [RCV004918010]	uncertain significance	10	114300325	114300325	Human		name
597642419	CV3663503	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1363T>C (p.Phe455Leu)	not specified [RCV004909345]	uncertain significance	10	114302406	114302406	Human		name
598162513	CV3953149	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1604G>A (p.Arg535Gln)	not specified [RCV005329184]	uncertain significance	10	114300629	114300629	Human		name
598171450	CV3953176	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1679C>T (p.Pro560Leu)	not specified [RCV005331185]	uncertain significance	10	114300554	114300554	Human		name
598171493	CV3953182	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1945G>A (p.Val649Met)	not specified [RCV005331191]	uncertain significance	10	114300206	114300206	Human		name
598171516	CV3953187	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1133A>G (p.Asn378Ser)	not specified [RCV005331196]	likely benign	10	114304870	114304870	Human		name
598171642	CV3953211	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1999C>T (p.Arg667Trp)	not specified [RCV005331220]	uncertain significance	10	114299374	114299374	Human		name
598171692	CV3953222	single nucleotide variant	NM_001001936.3(AFAP1L2):c.1151A>G (p.Gln384Arg)	not specified [RCV005331231]	uncertain significance	10	114304852	114304852	Human		name

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