Atg9b Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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96 records found for search term Atg9b

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156118035	CV2349522	single nucleotide variant	NM_001317056.2(ATG9B):c.23G>C (p.Gly8Ala)	not specified [RCV004201486]	uncertain significance	7	151024401	151024401	Human		name
329393366	CV2466891	single nucleotide variant	NM_001317056.2(ATG9B):c.19T>C (p.Trp7Arg)	not specified [RCV004282662]	uncertain significance	7	151024405	151024405	Human		name
401769789	CV2689940	single nucleotide variant	NM_001317056.2(ATG9B):c.21G>T (p.Trp7Cys)	not specified [RCV004297827]	uncertain significance	7	151024403	151024403	Human		name
405701106	CV3279940	single nucleotide variant	NM_001317056.2(ATG9B):c.20G>T (p.Trp7Leu)	not specified [RCV004425422]	uncertain significance	7	151024404	151024404	Human		name
407486744	CV3485056	single nucleotide variant	NM_001317056.2(ATG9B):c.23G>T (p.Gly8Val)	not specified [RCV004670568]	uncertain significance	7	151024401	151024401	Human		name
156032599	CV2376509	single nucleotide variant	NM_001317056.2(ATG9B):c.71C>T (p.Ser24Leu)	not specified [RCV004220681]	uncertain significance	7	151024353	151024353	Human		name
597702074	CV3603084	single nucleotide variant	NM_001317056.2(ATG9B):c.46C>T (p.Arg16Trp)	not specified [RCV004860055]	uncertain significance	7	151024378	151024378	Human		name
598242633	CV3914769	single nucleotide variant	NM_001317056.2(ATG9B):c.76C>T (p.Pro26Ser)	not specified [RCV005276568]	uncertain significance	7	151024348	151024348	Human		name
156357519	CV2254039	single nucleotide variant	NM_001317056.2(ATG9B):c.185C>T (p.Ser62Phe)	not specified [RCV004129490]	uncertain significance	7	151024239	151024239	Human		name
156195081	CV2347416	single nucleotide variant	NM_001317056.2(ATG9B):c.253C>A (p.Gln85Lys)	not specified [RCV004207254]	uncertain significance	7	151024171	151024171	Human		name
401752285	CV2682768	single nucleotide variant	NM_001317056.2(ATG9B):c.283G>A (p.Ala95Thr)	not specified [RCV004281742]	uncertain significance	7	151024141	151024141	Human		name
401923945	CV2823341	single nucleotide variant	NM_001317056.2(ATG9B):c.1329C>T (p.Ala443=)	not provided [RCV003435300]	likely benign	7	151019009	151019009	Human		name
401923943	CV2823342	single nucleotide variant	NM_001317056.2(ATG9B):c.1048C>A (p.Arg350=)	not provided [RCV003435301]	likely benign	7	151019290	151019290	Human		name
401909154	CV2823343	single nucleotide variant	NM_001317056.2(ATG9B):c.1047G>A (p.Pro349=)	not provided [RCV003423831]	likely benign	7	151019291	151019291	Human		name
405701121	CV3279942	single nucleotide variant	NM_001317056.2(ATG9B):c.260G>T (p.Cys87Phe)	not specified [RCV004425424]	uncertain significance	7	151024164	151024164	Human		name
407486763	CV3485076	single nucleotide variant	NM_001317056.2(ATG9B):c.290C>T (p.Pro97Leu)	not specified [RCV004670584]	uncertain significance	7	151024134	151024134	Human		name
597765299	CV3603121	single nucleotide variant	NM_001317056.2(ATG9B):c.184T>G (p.Ser62Ala)	not specified [RCV004870337]	uncertain significance	7	151024240	151024240	Human		name
598170195	CV3914721	single nucleotide variant	NM_001317056.2(ATG9B):c.292C>A (p.Pro98Thr)	not specified [RCV005284508]	uncertain significance	7	151024132	151024132	Human		name
598242520	CV3914737	single nucleotide variant	NM_001317056.2(ATG9B):c.215G>T (p.Gly72Val)	not specified [RCV005276545]	uncertain significance	7	151024209	151024209	Human		name
598242553	CV3914751	single nucleotide variant	NM_001317056.2(ATG9B):c.292C>G (p.Pro98Ala)	not specified [RCV005276553]	uncertain significance	7	151024132	151024132	Human		name
156149873	CV2201048	single nucleotide variant	NM_001317056.2(ATG9B):c.758G>A (p.Gly253Glu)	not specified [RCV004074810]	uncertain significance	7	151023108	151023108	Human		name
156400981	CV2213681	single nucleotide variant	NM_001317056.2(ATG9B):c.613C>T (p.Arg205Trp)	not specified [RCV004089757]	uncertain significance	7	151023491	151023491	Human		name
156026192	CV2242325	single nucleotide variant	NM_001317056.2(ATG9B):c.747T>G (p.His249Gln)	not specified [RCV004111339]	uncertain significance	7	151023119	151023119	Human		name
155978286	CV2247027	single nucleotide variant	NM_001317056.2(ATG9B):c.673A>T (p.Ile225Phe)	not specified [RCV004114587]	uncertain significance	7	151023193	151023193	Human		name
156183096	CV2295636	single nucleotide variant	NM_001317056.2(ATG9B):c.931G>C (p.Val311Leu)	not specified [RCV004149802]	uncertain significance	7	151021220	151021220	Human		name
156395650	CV2329305	single nucleotide variant	NM_001317056.2(ATG9B):c.361C>A (p.Pro121Thr)	not specified [RCV004174037]	uncertain significance	7	151024063	151024063	Human		name
156007301	CV2365140	single nucleotide variant	NM_001317056.2(ATG9B):c.371C>G (p.Pro124Arg)	not specified [RCV004205163]	uncertain significance	7	151024053	151024053	Human		name
156038264	CV2384157	single nucleotide variant	NM_001317056.2(ATG9B):c.835C>T (p.Pro279Ser)	not specified [RCV004227557]	uncertain significance	7	151021316	151021316	Human		name
156090968	CV2389399	single nucleotide variant	NM_001317056.2(ATG9B):c.352T>C (p.Ser118Pro)	not specified [RCV004238134]	uncertain significance	7	151024072	151024072	Human		name
329357402	CV2427706	single nucleotide variant	NM_001317056.2(ATG9B):c.331T>G (p.Ser111Ala)	not specified [RCV004252491]	uncertain significance	7	151024093	151024093	Human		name
329352471	CV2453065	single nucleotide variant	NM_001317056.2(ATG9B):c.815C>G (p.Ala272Gly)	not specified [RCV004277675]	uncertain significance	7	151023051	151023051	Human		name
329379161	CV2460195	single nucleotide variant	NM_001317056.2(ATG9B):c.530A>C (p.His177Pro)	not specified [RCV004273292]	uncertain significance	7	151023894	151023894	Human		name
401731005	CV2674228	single nucleotide variant	NM_001317056.2(ATG9B):c.716A>T (p.Asn239Ile)	not specified [RCV004289118]	uncertain significance	7	151023150	151023150	Human		name
401730235	CV2680057	single nucleotide variant	NM_001317056.2(ATG9B):c.431C>T (p.Pro144Leu)	not specified [RCV004286553]	uncertain significance	7	151023993	151023993	Human		name
401744380	CV2680950	single nucleotide variant	NM_001317056.2(ATG9B):c.701G>C (p.Arg234Pro)	not specified [RCV004296022]	uncertain significance	7	151023165	151023165	Human		name
401729624	CV2690385	single nucleotide variant	NM_001317056.2(ATG9B):c.487C>G (p.Gln163Glu)	not specified [RCV004302374]	uncertain significance	7	151023937	151023937	Human		name
401728620	CV2729696	single nucleotide variant	NM_001317056.2(ATG9B):c.713A>G (p.Tyr238Cys)	not specified [RCV004331953]	uncertain significance	7	151023153	151023153	Human		name
401878778	CV2754820	single nucleotide variant	NM_001317056.2(ATG9B):c.454G>A (p.Glu152Lys)	not specified [RCV004341298]	uncertain significance	7	151023970	151023970	Human		name
401855350	CV2757261	single nucleotide variant	NM_001317056.2(ATG9B):c.868G>A (p.Gly290Ser)	not specified [RCV004338853]	uncertain significance	7	151021283	151021283	Human		name
401855878	CV2757588	single nucleotide variant	NM_001317056.2(ATG9B):c.428G>A (p.Gly143Asp)	not specified [RCV004340956]	uncertain significance	7	151023996	151023996	Human		name
405701129	CV3279943	single nucleotide variant	NM_001317056.2(ATG9B):c.370C>T (p.Pro124Ser)	not specified [RCV004425425]	likely benign	7	151024054	151024054	Human		name
405701135	CV3279944	single nucleotide variant	NM_001317056.2(ATG9B):c.400C>T (p.Pro134Ser)	not specified [RCV004425426]	uncertain significance	7	151024024	151024024	Human		name
405701147	CV3279946	single nucleotide variant	NM_001317056.2(ATG9B):c.575T>C (p.Leu192Pro)	not specified [RCV004425428]	uncertain significance	7	151023706	151023706	Human		name
405701151	CV3279947	single nucleotide variant	NM_001317056.2(ATG9B):c.761C>T (p.Pro254Leu)	not specified [RCV004425429]	likely benign	7	151023105	151023105	Human		name
407487930	CV3485046	single nucleotide variant	NM_001317056.2(ATG9B):c.902G>A (p.Cys301Tyr)	not specified [RCV004679202]	uncertain significance	7	151021249	151021249	Human		name
407486751	CV3485059	single nucleotide variant	NM_001317056.2(ATG9B):c.854T>C (p.Leu285Pro)	not specified [RCV004670571]	uncertain significance	7	151021297	151021297	Human		name
407486768	CV3485078	single nucleotide variant	NM_001317056.2(ATG9B):c.541G>A (p.Gly181Arg)	not specified [RCV004670586]	uncertain significance	7	151023883	151023883	Human		name
597765316	CV3599676	single nucleotide variant	NM_001317056.2(ATG9B):c.701G>A (p.Arg234Gln)	not specified [RCV004870341]	uncertain significance	7	151023165	151023165	Human		name
597765370	CV3599695	single nucleotide variant	NM_001317056.2(ATG9B):c.410C>A (p.Ser137Tyr)	not specified [RCV004870355]	uncertain significance	7	151024014	151024014	Human		name
597702545	CV3599732	single nucleotide variant	NM_001317056.2(ATG9B):c.626C>G (p.Ala209Gly)	not specified [RCV004860101]	uncertain significance	7	151023478	151023478	Human		name
597702675	CV3599763	single nucleotide variant	NM_001317056.2(ATG9B):c.947C>T (p.Ala316Val)	not specified [RCV004860114]	uncertain significance	7	151021204	151021204	Human		name
597702174	CV3603113	single nucleotide variant	NM_001317056.2(ATG9B):c.826C>T (p.Arg276Cys)	not specified [RCV004860066]	uncertain significance	7	151021325	151021325	Human		name
156317907	CV2200205	single nucleotide variant	NM_001317056.2(ATG9B):c.1870G>C (p.Ala624Pro)	not specified [RCV004076556]	uncertain significance	7	151018296	151018296	Human		name
156373769	CV2201399	single nucleotide variant	NM_001317056.2(ATG9B):c.1901C>G (p.Pro634Arg)	not specified [RCV004077518]	uncertain significance	7	151018022	151018022	Human		name
156244861	CV2231637	single nucleotide variant	NM_001317056.2(ATG9B):c.1417C>T (p.Pro473Ser)	not specified [RCV004098208]	uncertain significance	7	151018921	151018921	Human		name
156271149	CV2237113	single nucleotide variant	NM_001317056.2(ATG9B):c.2077G>C (p.Ala693Pro)	not specified [RCV004114867]	uncertain significance	7	151017248	151017248	Human		name
156197335	CV2241611	single nucleotide variant	NM_001317056.2(ATG9B):c.2029G>A (p.Val677Met)	not specified [RCV004104496]	uncertain significance	7	151017894	151017894	Human		name
156087220	CV2258972	single nucleotide variant	NM_001317056.2(ATG9B):c.1019A>G (p.Gln340Arg)	not specified [RCV004120246]	uncertain significance	7	151019319	151019319	Human		name
155970677	CV2262265	single nucleotide variant	NM_001317056.2(ATG9B):c.1793A>G (p.His598Arg)	not specified [RCV004128472]	uncertain significance	7	151018373	151018373	Human		name
156396213	CV2326158	single nucleotide variant	NM_001317056.2(ATG9B):c.1063C>G (p.Leu355Val)	not specified [RCV004180428]	uncertain significance	7	151019275	151019275	Human		name
156004098	CV2357525	single nucleotide variant	NM_001317056.2(ATG9B):c.1409G>A (p.Arg470Gln)	not specified [RCV004202801]	uncertain significance	7	151018929	151018929	Human		name
156134529	CV2362064	single nucleotide variant	NM_001317056.2(ATG9B):c.2111C>G (p.Thr704Ser)	not specified [RCV004209875]	uncertain significance	7	151017214	151017214	Human		name
329381087	CV2440638	single nucleotide variant	NM_001317056.2(ATG9B):c.1790T>C (p.Met597Thr)	not specified [RCV004256548]	uncertain significance	7	151018376	151018376	Human		name
329391594	CV2452955	single nucleotide variant	NM_001317056.2(ATG9B):c.1535C>T (p.Ala512Val)	not specified [RCV004277585]	uncertain significance	7	151018803	151018803	Human		name
329390277	CV2453845	single nucleotide variant	NM_001317056.2(ATG9B):c.1873G>T (p.Val625Phe)	not specified [RCV004271244]	uncertain significance	7	151018050	151018050	Human		name
329390551	CV2455289	single nucleotide variant	NM_001317056.2(ATG9B):c.1256C>T (p.Pro419Leu)	not specified [RCV004274800]	uncertain significance	7	151019082	151019082	Human		name
329377889	CV2458947	single nucleotide variant	NM_001317056.2(ATG9B):c.1517C>T (p.Ala506Val)	not specified [RCV004272440]	uncertain significance	7	151018821	151018821	Human		name
401726657	CV2695752	single nucleotide variant	NM_001317056.2(ATG9B):c.1417C>G (p.Pro473Ala)	not specified [RCV004299549]	uncertain significance	7	151018921	151018921	Human		name
401771984	CV2723012	single nucleotide variant	NM_001317056.2(ATG9B):c.1759C>G (p.Gln587Glu)	not specified [RCV004327183]	uncertain significance	7	151018407	151018407	Human		name
401884873	CV2774883	single nucleotide variant	NM_001317056.2(ATG9B):c.1006C>T (p.Leu336Phe)	not specified [RCV004343963]	uncertain significance	7	151019332	151019332	Human		name
405701083	CV3279936	single nucleotide variant	NM_001317056.2(ATG9B):c.1352C>T (p.Pro451Leu)	not specified [RCV004425418]	uncertain significance	7	151018986	151018986	Human		name
405701095	CV3279938	single nucleotide variant	NM_001317056.2(ATG9B):c.1556C>T (p.Pro519Leu)	not specified [RCV004425420]	uncertain significance	7	151018782	151018782	Human		name
405701099	CV3279939	single nucleotide variant	NM_001317056.2(ATG9B):c.1637C>A (p.Thr546Asn)	not specified [RCV004425421]	uncertain significance	7	151018701	151018701	Human		name
407487925	CV3485036	single nucleotide variant	NM_001317056.2(ATG9B):c.2093G>A (p.Arg698His)	not specified [RCV004679199]	uncertain significance	7	151017232	151017232	Human		name
407487937	CV3485063	single nucleotide variant	NM_001317056.2(ATG9B):c.1310G>A (p.Arg437His)	not specified [RCV004679207]	uncertain significance	7	151019028	151019028	Human		name
407486757	CV3485072	single nucleotide variant	NM_001317056.2(ATG9B):c.2060C>T (p.Ser687Leu)	not specified [RCV004670581]	uncertain significance	7	151017265	151017265	Human		name
407486773	CV3485083	single nucleotide variant	NM_001317056.2(ATG9B):c.1162A>G (p.Ser388Gly)	not specified [RCV004670591]	uncertain significance	7	151019176	151019176	Human		name
407486778	CV3485090	single nucleotide variant	NM_001317056.2(ATG9B):c.1411C>T (p.Arg471Cys)	not specified [RCV004670597]	uncertain significance	7	151018927	151018927	Human		name
597765343	CV3599685	single nucleotide variant	NM_001317056.2(ATG9B):c.1066G>C (p.Asp356His)	not specified [RCV004870348]	uncertain significance	7	151019272	151019272	Human		name
597765857	CV3599703	single nucleotide variant	NM_001317056.2(ATG9B):c.1386C>G (p.Phe462Leu)	not specified [RCV004870359]	uncertain significance	7	151018952	151018952	Human		name
597765842	CV3599712	single nucleotide variant	NM_001317056.2(ATG9B):c.1522C>G (p.Arg508Gly)	not specified [RCV004870363]	uncertain significance	7	151018816	151018816	Human		name
597702501	CV3599722	single nucleotide variant	NM_001317056.2(ATG9B):c.1222C>T (p.Pro408Ser)	not specified [RCV004860097]	uncertain significance	7	151019116	151019116	Human		name
597702594	CV3599743	single nucleotide variant	NM_001317056.2(ATG9B):c.1802C>G (p.Pro601Arg)	not specified [RCV004860106]	uncertain significance	7	151018364	151018364	Human		name
597765393	CV3599754	single nucleotide variant	NM_001317056.2(ATG9B):c.2012C>G (p.Ser671Cys)	not specified [RCV004870385]	uncertain significance	7	151017911	151017911	Human		name
597765433	CV3599774	single nucleotide variant	NM_001317056.2(ATG9B):c.1816C>G (p.Pro606Ala)	not specified [RCV004870396]	likely benign	7	151018350	151018350	Human		name
597702740	CV3599784	single nucleotide variant	NM_001317056.2(ATG9B):c.1940C>T (p.Pro647Leu)	not specified [RCV004860123]	uncertain significance	7	151017983	151017983	Human		name
597702143	CV3603104	single nucleotide variant	NM_001317056.2(ATG9B):c.1696G>A (p.Gly566Arg)	not specified [RCV004860063]	uncertain significance	7	151018642	151018642	Human		name
598170147	CV3914702	single nucleotide variant	NM_001317056.2(ATG9B):c.1310G>T (p.Arg437Leu)	not specified [RCV005284492]	uncertain significance	7	151019028	151019028	Human		name
598237079	CV3914712	single nucleotide variant	NM_001317056.2(ATG9B):c.1558C>G (p.Pro520Ala)	not specified [RCV005275584]	uncertain significance	7	151018780	151018780	Human		name
598242672	CV3914776	single nucleotide variant	NM_001317056.2(ATG9B):c.2035C>A (p.Arg679Ser)	not specified [RCV005276575]	uncertain significance	7	151017888	151017888	Human		name
598242730	CV3914785	single nucleotide variant	NM_001317056.2(ATG9B):c.1912C>T (p.Pro638Ser)	not specified [RCV005276584]	uncertain significance	7	151018011	151018011	Human		name
598242777	CV3914795	single nucleotide variant	NM_001317056.2(ATG9B):c.1550C>G (p.Ala517Gly)	not specified [RCV005276592]	uncertain significance	7	151018788	151018788	Human		name
598237138	CV3914806	single nucleotide variant	NM_001317056.2(ATG9B):c.1516G>C (p.Ala506Pro)	not specified [RCV005275598]	uncertain significance	7	151018822	151018822	Human		name
598242884	CV3914817	single nucleotide variant	NM_001317056.2(ATG9B):c.1286G>A (p.Gly429Asp)	not specified [RCV005276611]	uncertain significance	7	151019052	151019052	Human		name
598242947	CV3914828	single nucleotide variant	NM_001317056.2(ATG9B):c.1510G>T (p.Ala504Ser)	not specified [RCV005276621]	uncertain significance	7	151018828	151018828	Human		name
40903973	CV918073	single nucleotide variant	NM_001317056.2(ATG9B):c.1480G>T (p.Glu494Ter)	Premature ovarian failure [RCV001270209]	likely pathogenic	7	151018858	151018858	Human	2	name

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