Atg16l2 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for All species
(View Results for all Objects and Ontologies)

64 records found for search term Atg16l2

Refine Term:

Sort By:

Export

CSV

TAB

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

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Create Name:

Description:

Send us a Message