Atg16l2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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64 records found for search term Atg16l2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155902372	CV2301426	single nucleotide variant	NM_033388.2(ATG16L2):c.22G>A (p.Gly8Ser)	not specified [RCV004162361]	uncertain significance	11	72814467	72814467	Human		name
598268039	CV3921532	single nucleotide variant	NM_033388.2(ATG16L2):c.17T>C (p.Val6Ala)	not specified [RCV005281693]	uncertain significance	11	72814462	72814462	Human		name
407495020	CV3474301	single nucleotide variant	NM_033388.2(ATG16L2):c.37C>T (p.Arg13Cys)	not specified [RCV004667777]	uncertain significance	11	72814482	72814482	Human		name
598267988	CV3921522	single nucleotide variant	NM_033388.2(ATG16L2):c.54C>G (p.Ile18Met)	not specified [RCV005281684]	uncertain significance	11	72814499	72814499	Human		name
156103349	CV2291601	single nucleotide variant	NM_033388.2(ATG16L2):c.262G>A (p.Ala88Thr)	not specified [RCV004155897]	likely benign	11	72817799	72817799	Human		name
329367860	CV2427616	single nucleotide variant	NM_033388.2(ATG16L2):c.206A>G (p.His69Arg)	not specified [RCV004250248]	uncertain significance	11	72816815	72816815	Human		name
401909703	CV2813518	single nucleotide variant	NM_033388.2(ATG16L2):c.1344G>A (p.Glu448=)	not provided [RCV003398122]	likely benign	11	72826801	72826801	Human		name
405688805	CV3279792	single nucleotide variant	NM_033388.2(ATG16L2):c.125A>G (p.His42Arg)	not specified [RCV004423291]	likely benign	11	72816734	72816734	Human		name
405688810	CV3279793	single nucleotide variant	NM_033388.2(ATG16L2):c.127C>G (p.Leu43Val)	not specified [RCV004423292]	uncertain significance	11	72816736	72816736	Human		name
405688823	CV3279796	single nucleotide variant	NM_033388.2(ATG16L2):c.176C>T (p.Pro59Leu)	not specified [RCV004423295]	uncertain significance	11	72816785	72816785	Human		name
405688828	CV3279797	single nucleotide variant	NM_033388.2(ATG16L2):c.1773C>T (p.Cys591=)	not specified [RCV004423296]	likely benign	11	72829303	72829303	Human		name
597677349	CV3596432	single nucleotide variant	NM_033388.2(ATG16L2):c.209A>G (p.Gln70Arg)	not specified [RCV004857060]	uncertain significance	11	72816818	72816818	Human		name
597677777	CV3596479	single nucleotide variant	NM_033388.2(ATG16L2):c.1473G>A (p.Arg491=)	not specified [RCV004857103]	likely benign	11	72828359	72828359	Human		name
597677882	CV3596489	single nucleotide variant	NM_033388.2(ATG16L2):c.139G>C (p.Ala47Pro)	not specified [RCV004857113]	uncertain significance	11	72816748	72816748	Human		name
156142099	CV2199989	single nucleotide variant	NM_033388.2(ATG16L2):c.848C>T (p.Thr283Met)	not specified [RCV004074153]	uncertain significance	11	72824083	72824083	Human		name
156095972	CV2210347	single nucleotide variant	NM_033388.2(ATG16L2):c.368C>T (p.Ser123Leu)	not specified [RCV004089502]	uncertain significance	11	72821717	72821717	Human		name
156244277	CV2243078	single nucleotide variant	NM_033388.2(ATG16L2):c.829G>C (p.Ala277Pro)	not specified [RCV004109993]	uncertain significance	11	72824064	72824064	Human		name
156136434	CV2245705	single nucleotide variant	NM_033388.2(ATG16L2):c.748A>G (p.Arg250Gly)	not specified [RCV004111582]	uncertain significance	11	72822885	72822885	Human		name
155930214	CV2299808	single nucleotide variant	NM_033388.2(ATG16L2):c.656C>T (p.Ala219Val)	not specified [RCV004148963]	uncertain significance	11	72822489	72822489	Human		name
156343222	CV2364080	single nucleotide variant	NM_033388.2(ATG16L2):c.586G>C (p.Val196Leu)	not specified [RCV004221463]	uncertain significance	11	72822237	72822237	Human		name
156387401	CV2372733	single nucleotide variant	NM_033388.2(ATG16L2):c.563C>G (p.Ala188Gly)	not specified [RCV004221924]	uncertain significance	11	72822214	72822214	Human		name
329374061	CV2434684	single nucleotide variant	NM_033388.2(ATG16L2):c.979C>T (p.Arg327Trp)	not specified [RCV004248401]	uncertain significance	11	72824825	72824825	Human		name
401866071	CV2762512	single nucleotide variant	NM_033388.2(ATG16L2):c.622C>G (p.Leu208Val)	not specified [RCV004338047]	uncertain significance	11	72822273	72822273	Human		name
401865128	CV2791502	single nucleotide variant	NM_033388.2(ATG16L2):c.950C>G (p.Pro317Arg)	not specified [RCV004358885]	uncertain significance	11	72824796	72824796	Human		name
405688838	CV3279799	single nucleotide variant	NM_033388.2(ATG16L2):c.494C>A (p.Ala165Glu)	not specified [RCV004423298]	uncertain significance	11	72822145	72822145	Human		name
405688843	CV3279800	single nucleotide variant	NM_033388.2(ATG16L2):c.597G>C (p.Lys199Asn)	not specified [RCV004423299]	uncertain significance	11	72822248	72822248	Human		name
405688849	CV3279801	single nucleotide variant	NM_033388.2(ATG16L2):c.914T>C (p.Ile305Thr)	not specified [RCV004423300]	uncertain significance	11	72824760	72824760	Human		name
407494946	CV3474277	single nucleotide variant	NM_033388.2(ATG16L2):c.851T>C (p.Leu284Pro)	not specified [RCV004667758]	uncertain significance	11	72824086	72824086	Human		name
407494969	CV3474285	single nucleotide variant	NM_033388.2(ATG16L2):c.415G>C (p.Val139Leu)	not specified [RCV004667765]	uncertain significance	11	72822066	72822066	Human		name
407494992	CV3474291	single nucleotide variant	NM_033388.2(ATG16L2):c.968G>A (p.Arg323Gln)	not specified [RCV004667770]	uncertain significance	11	72824814	72824814	Human		name
407494999	CV3474294	single nucleotide variant	NM_033388.2(ATG16L2):c.845T>G (p.Leu282Arg)	not specified [RCV004667772]	uncertain significance	11	72824080	72824080	Human		name
407495112	CV3474330	single nucleotide variant	NM_033388.2(ATG16L2):c.448G>T (p.Ala150Ser)	not specified [RCV004667798]	uncertain significance	11	72822099	72822099	Human		name
597677338	CV3596423	single nucleotide variant	NM_033388.2(ATG16L2):c.673C>G (p.Leu225Val)	not specified [RCV004857059]	uncertain significance	11	72822506	72822506	Human		name
597677427	CV3596441	single nucleotide variant	NM_033388.2(ATG16L2):c.470G>T (p.Arg157Leu)	not specified [RCV004857068]	uncertain significance	11	72822121	72822121	Human		name
597677612	CV3596460	single nucleotide variant	NM_033388.2(ATG16L2):c.626G>A (p.Arg209His)	not specified [RCV004857087]	uncertain significance	11	72822277	72822277	Human		name
597677998	CV3596500	single nucleotide variant	NM_033388.2(ATG16L2):c.568G>T (p.Asp190Tyr)	not specified [RCV004857124]	uncertain significance	11	72822219	72822219	Human		name
598199821	CV3911116	single nucleotide variant	NM_033388.2(ATG16L2):c.455A>G (p.Gln152Arg)	not specified [RCV005268452]	uncertain significance	11	72822106	72822106	Human		name
15117401	CV713154	single nucleotide variant	NM_033388.2(ATG16L2):c.956G>C (p.Cys319Ser)	not provided [RCV000962198]	benign	11	72824802	72824802	Human		name
156032749	CV2214513	single nucleotide variant	NM_033388.2(ATG16L2):c.1455C>G (p.Ile485Met)	not specified [RCV004088567]	uncertain significance	11	72827276	72827276	Human		name
156221107	CV2222455	single nucleotide variant	NM_033388.2(ATG16L2):c.1736C>T (p.Thr579Ile)	not specified [RCV004099309]	uncertain significance	11	72828948	72828948	Human		name
155992594	CV2253483	single nucleotide variant	NM_033388.2(ATG16L2):c.1298C>T (p.Thr433Met)	not specified [RCV004599493]	uncertain significance	11	72826755	72826755	Human		name
156209014	CV2298171	single nucleotide variant	NM_033388.2(ATG16L2):c.1816A>G (p.Met606Val)	not specified [RCV004159829]	likely benign	11	72829346	72829346	Human		name
156162237	CV2319538	single nucleotide variant	NM_033388.2(ATG16L2):c.1073G>A (p.Arg358His)	not specified [RCV004185103]	uncertain significance	11	72825378	72825378	Human		name
156059182	CV2343687	single nucleotide variant	NM_033388.2(ATG16L2):c.1807G>A (p.Gly603Arg)	not specified [RCV004190712]	uncertain significance	11	72829337	72829337	Human		name
156163451	CV2368471	single nucleotide variant	NM_033388.2(ATG16L2):c.1331G>A (p.Arg444Gln)	not specified [RCV004221274]	uncertain significance	11	72826788	72826788	Human		name
156224909	CV2390442	single nucleotide variant	NM_033388.2(ATG16L2):c.1738G>A (p.Gly580Arg)	not specified [RCV004238985]	uncertain significance	11	72828950	72828950	Human		name
329377564	CV2462665	single nucleotide variant	NM_033388.2(ATG16L2):c.1565G>A (p.Arg522Gln)	not specified [RCV004278600]	uncertain significance	11	72828451	72828451	Human		name
329364276	CV2467377	single nucleotide variant	NM_033388.2(ATG16L2):c.1253T>C (p.Leu418Pro)	not specified [RCV004285165]	uncertain significance	11	72826710	72826710	Human		name
401744146	CV2680901	single nucleotide variant	NM_033388.2(ATG16L2):c.1027C>G (p.Arg343Gly)	not specified [RCV004295976]	uncertain significance	11	72825332	72825332	Human		name
401874143	CV2754590	single nucleotide variant	NM_033388.2(ATG16L2):c.1324C>T (p.Arg442Cys)	not specified [RCV004339267]	uncertain significance	11	72826781	72826781	Human		name
401894374	CV2780850	single nucleotide variant	NM_033388.2(ATG16L2):c.1482C>A (p.His494Gln)	not specified [RCV004352162]	uncertain significance	11	72828368	72828368	Human		name
401896938	CV2785424	single nucleotide variant	NM_033388.2(ATG16L2):c.1514T>C (p.Val505Ala)	not specified [RCV004362967]	uncertain significance	11	72828400	72828400	Human		name
405688795	CV3279790	single nucleotide variant	NM_033388.2(ATG16L2):c.1124C>T (p.Thr375Ile)	not specified [RCV004423289]	uncertain significance	11	72826194	72826194	Human		name
405688800	CV3279791	single nucleotide variant	NM_033388.2(ATG16L2):c.1229G>A (p.Gly410Glu)	not specified [RCV004423290]	uncertain significance	11	72826573	72826573	Human		name
405688819	CV3279795	single nucleotide variant	NM_033388.2(ATG16L2):c.1426A>T (p.Ile476Phe)	not specified [RCV004423294]	uncertain significance	11	72827247	72827247	Human		name
405688832	CV3279798	single nucleotide variant	NM_033388.2(ATG16L2):c.1838G>C (p.Arg613Thr)	not specified [RCV004423297]	uncertain significance	11	72829368	72829368	Human		name
407495036	CV3474309	single nucleotide variant	NM_033388.2(ATG16L2):c.1325G>A (p.Arg442His)	not specified [RCV004667781]	uncertain significance	11	72826782	72826782	Human		name
407495068	CV3474319	single nucleotide variant	NM_033388.2(ATG16L2):c.1703G>A (p.Cys568Tyr)	not specified [RCV004667789]	likely benign	11	72828915	72828915	Human		name
597677517	CV3596450	single nucleotide variant	NM_033388.2(ATG16L2):c.1627G>A (p.Asp543Asn)	not specified [RCV004857077]	uncertain significance	11	72828733	72828733	Human		name
597677668	CV3596468	single nucleotide variant	NM_033388.2(ATG16L2):c.1354G>A (p.Gly452Ser)	not specified [RCV004857092]	uncertain significance	11	72826811	72826811	Human		name
598267815	CV3911126	single nucleotide variant	NM_033388.2(ATG16L2):c.1789G>A (p.Val597Met)	not specified [RCV005281655]	uncertain significance	11	72829319	72829319	Human		name
598267869	CV3921501	single nucleotide variant	NM_033388.2(ATG16L2):c.1792G>A (p.Ala598Thr)	not specified [RCV005281664]	uncertain significance	11	72829322	72829322	Human		name
598267927	CV3921512	single nucleotide variant	NM_033388.2(ATG16L2):c.1357C>T (p.Arg453Cys)	not specified [RCV005281674]	uncertain significance	11	72826814	72826814	Human		name
598268083	CV3921542	single nucleotide variant	NM_033388.2(ATG16L2):c.1510C>T (p.Arg504Trp)	not specified [RCV005281701]	uncertain significance	11	72828396	72828396	Human		name

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