Ulk1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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144 records found for search term Ulk1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15199441	CV760118	single nucleotide variant	NM_003565.4(ULK1):c.2183-3C>T	not provided [RCV000912548]	benign	12	131917408	131917408	Human		name
15144896	CV759967	single nucleotide variant	NM_003565.4(ULK1):c.2684+10G>A	not provided [RCV000922447]	likely benign	12	131919394	131919394	Human		name
401909980	CV2817149	single nucleotide variant	NM_003565.4(ULK1):c.135C>T (p.Val45=)	not provided [RCV003398281]	likely benign	12	131895624	131895624	Human		name
405805476	CV3348216	single nucleotide variant	NM_003565.4(ULK1):c.52C>T (p.Arg18Cys)	not specified [RCV004479737]	uncertain significance	12	131895053	131895053	Human		name
407523501	CV3489202	single nucleotide variant	NM_003565.4(ULK1):c.66C>G (p.Ile22Met)	not specified [RCV004678086]	uncertain significance	12	131895067	131895067	Human		name
598266456	CV3925471	single nucleotide variant	NM_003565.4(ULK1):c.43G>C (p.Glu15Gln)	not specified [RCV005301944]	uncertain significance	12	131895044	131895044	Human		name
15117908	CV717941	single nucleotide variant	NM_003565.4(ULK1):c.648G>A (p.Thr216=)	not provided [RCV000962282]	benign	12	131909219	131909219	Human		name
401909982	CV2817150	single nucleotide variant	NM_003565.4(ULK1):c.1179G>T (p.Ala393=)	not provided [RCV003398282]	likely benign	12	131913768	131913768	Human		name
401909984	CV2817151	single nucleotide variant	NM_003565.4(ULK1):c.2292G>A (p.Thr764=)	not provided [RCV003398283]	likely benign	12	131917520	131917520	Human		name
405805426	CV3348193	single nucleotide variant	NM_003565.4(ULK1):c.100C>T (p.Arg34Cys)	not specified [RCV004479714]	uncertain significance	12	131895101	131895101	Human		name
597790070	CV3632617	single nucleotide variant	NM_003565.4(ULK1):c.223A>G (p.Ile75Val)	not specified [RCV004876254]	uncertain significance	12	131895801	131895801	Human		name
15160556	CV706401	single nucleotide variant	NM_003565.4(ULK1):c.1788G>A (p.Leu596=)	not provided [RCV000947508]	benign	12	131916069	131916069	Human		name
15178537	CV706402	single nucleotide variant	NM_003565.4(ULK1):c.2271C>A (p.Gly757=)	not provided [RCV000951304]	benign	12	131917499	131917499	Human		name
15155374	CV717944	single nucleotide variant	NM_003565.4(ULK1):c.2778C>T (p.Leu926=)	not provided [RCV000968913]	benign	12	131919565	131919565	Human		name
15155379	CV717945	single nucleotide variant	NM_003565.4(ULK1):c.2871G>A (p.Leu957=)	not provided [RCV000968914]	benign\|likely benign	12	131920046	131920046	Human		name
15124846	CV717946	single nucleotide variant	NM_003565.4(ULK1):c.2896C>A (p.Arg966=)	not provided [RCV000963482]	benign	12	131920071	131920071	Human		name
15099108	CV729792	single nucleotide variant	NM_003565.4(ULK1):c.2769C>T (p.Ala923=)	not provided [RCV000891883]	benign	12	131919556	131919556	Human		name
15145364	CV743549	single nucleotide variant	NM_003565.4(ULK1):c.1722C>G (p.Pro574=)	not provided [RCV000900150]	benign\|likely benign	12	131916003	131916003	Human		name
156238036	CV2193605	single nucleotide variant	NM_003565.4(ULK1):c.821A>G (p.His274Arg)	not specified [RCV004074211]	uncertain significance	12	131910266	131910266	Human		name
156059009	CV2343669	single nucleotide variant	NM_003565.4(ULK1):c.901G>A (p.Gly301Ser)	not specified [RCV004190695]	uncertain significance	12	131910753	131910753	Human		name
156138058	CV2374190	single nucleotide variant	NM_003565.4(ULK1):c.958G>A (p.Glu320Lys)	not specified [RCV004229335]	uncertain significance	12	131911951	131911951	Human		name
401773216	CV2698135	single nucleotide variant	NM_003565.4(ULK1):c.317C>A (p.Ala106Asp)	not specified [RCV004302918]	uncertain significance	12	131908644	131908644	Human		name
401889827	CV2763431	single nucleotide variant	NM_003565.4(ULK1):c.527T>C (p.Met176Thr)	not specified [RCV004349320]	uncertain significance	12	131908934	131908934	Human		name
405258553	CV3203848	single nucleotide variant	NM_003565.4(ULK1):c.725C>T (p.Thr242Ile)	ULK1-related disorder [RCV003942015]	likely benign	12	131909833	131909833	Human		name , trait , alternate_id
405805478	CV3348217	single nucleotide variant	NM_003565.4(ULK1):c.947C>T (p.Pro316Leu)	not specified [RCV004479738]	uncertain significance	12	131910799	131910799	Human		name
407523496	CV3489199	single nucleotide variant	NM_003565.4(ULK1):c.470A>G (p.Asn157Ser)	not specified [RCV004678084]	uncertain significance	12	131908797	131908797	Human		name
407523499	CV3489201	single nucleotide variant	NM_003565.4(ULK1):c.788A>G (p.His263Arg)	not specified [RCV004678085]	uncertain significance	12	131909981	131909981	Human		name
597790046	CV3632609	single nucleotide variant	NM_003565.4(ULK1):c.944C>T (p.Pro315Leu)	not specified [RCV004876248]	uncertain significance	12	131910796	131910796	Human		name
597790058	CV3632613	single nucleotide variant	NM_003565.4(ULK1):c.785A>G (p.Asn262Ser)	not specified [RCV004876251]	uncertain significance	12	131909978	131909978	Human		name
598190801	CV3925461	single nucleotide variant	NM_003565.4(ULK1):c.847T>C (p.Ser283Pro)	not specified [RCV005288260]	uncertain significance	12	131910292	131910292	Human		name
598190825	CV3925469	single nucleotide variant	NM_003565.4(ULK1):c.956G>A (p.Gly319Asp)	not specified [RCV005288263]	uncertain significance	12	131911949	131911949	Human		name
598266452	CV3925470	single nucleotide variant	NM_003565.4(ULK1):c.397G>A (p.Gly133Ser)	not specified [RCV005301943]	uncertain significance	12	131908724	131908724	Human		name
156174987	CV2194477	single nucleotide variant	NM_003565.4(ULK1):c.2757C>G (p.Asp919Glu)	not specified [RCV004079570]	uncertain significance	12	131919544	131919544	Human		name
156372886	CV2204638	single nucleotide variant	NM_003565.4(ULK1):c.1637G>A (p.Arg546His)	not specified [RCV004081743]	likely benign	12	131915918	131915918	Human		name
156380137	CV2218064	single nucleotide variant	NM_003565.4(ULK1):c.2368G>T (p.Val790Leu)	not specified [RCV004086502]	uncertain significance	12	131918538	131918538	Human		name
156343046	CV2222609	single nucleotide variant	NM_003565.4(ULK1):c.2208C>A (p.Ser736Arg)	not specified [RCV004099436]	uncertain significance	12	131917436	131917436	Human		name
156224468	CV2229797	single nucleotide variant	NM_003565.4(ULK1):c.2164G>C (p.Glu722Gln)	not specified [RCV004105373]	uncertain significance	12	131917044	131917044	Human		name
156167051	CV2237205	single nucleotide variant	NM_003565.4(ULK1):c.1482G>A (p.Met494Ile)	not specified [RCV004114942]	uncertain significance	12	131915191	131915191	Human		name
156164529	CV2246804	single nucleotide variant	NM_003565.4(ULK1):c.2653G>A (p.Asp885Asn)	not specified [RCV004112331]	uncertain significance	12	131919353	131919353	Human		name
156149279	CV2265340	single nucleotide variant	NM_003565.4(ULK1):c.1310A>C (p.Gln437Pro)	not specified [RCV004128230]	uncertain significance	12	131914414	131914414	Human		name
155949726	CV2267709	single nucleotide variant	NM_003565.4(ULK1):c.2203G>A (p.Gly735Arg)	not specified [RCV004134246]	uncertain significance	12	131917431	131917431	Human		name
155904265	CV2275866	single nucleotide variant	NM_003565.4(ULK1):c.2278C>G (p.Pro760Ala)	not specified [RCV004139526]	uncertain significance	12	131917506	131917506	Human		name
156060896	CV2280293	single nucleotide variant	NM_003565.4(ULK1):c.1499G>A (p.Arg500Gln)	not specified [RCV004140494]	uncertain significance	12	131915208	131915208	Human		name
156251770	CV2286881	single nucleotide variant	NM_003565.4(ULK1):c.2368G>A (p.Val790Met)	not specified [RCV004142679]	uncertain significance	12	131918538	131918538	Human		name
156000526	CV2287394	single nucleotide variant	NM_003565.4(ULK1):c.1975C>T (p.Arg659Trp)	not specified [RCV004147002]	uncertain significance	12	131916494	131916494	Human		name
156082512	CV2292926	single nucleotide variant	NM_003565.4(ULK1):c.2056A>C (p.Lys686Gln)	not specified [RCV004148421]	uncertain significance	12	131916575	131916575	Human		name
156193258	CV2301955	single nucleotide variant	NM_003565.4(ULK1):c.2063C>T (p.Pro688Leu)	not specified [RCV004156730]	uncertain significance	12	131916582	131916582	Human		name
156058390	CV2305245	single nucleotide variant	NM_003565.4(ULK1):c.1745T>G (p.Phe582Cys)	not specified [RCV004171171]	uncertain significance	12	131916026	131916026	Human		name
156057229	CV2308996	single nucleotide variant	NM_003565.4(ULK1):c.1324C>G (p.Gln442Glu)	not specified [RCV004171061]	uncertain significance	12	131914428	131914428	Human		name
156095440	CV2310103	single nucleotide variant	NM_003565.4(ULK1):c.2693A>G (p.Glu898Gly)	not specified [RCV004163228]	uncertain significance	12	131919480	131919480	Human		name
155967556	CV2312738	single nucleotide variant	NM_003565.4(ULK1):c.2618G>A (p.Gly873Asp)	not specified [RCV004169460]	uncertain significance	12	131919318	131919318	Human		name
155963720	CV2330361	single nucleotide variant	NM_003565.4(ULK1):c.2599G>A (p.Ala867Thr)	not specified [RCV004180937]	uncertain significance	12	131919299	131919299	Human		name
156286839	CV2334970	single nucleotide variant	NM_003565.4(ULK1):c.2071C>T (p.Arg691Trp)	not specified [RCV004182067]	uncertain significance	12	131916590	131916590	Human		name
155970620	CV2338082	single nucleotide variant	NM_003565.4(ULK1):c.1841G>A (p.Arg614Gln)	not specified [RCV004186119]	uncertain significance	12	131916122	131916122	Human		name
155926458	CV2345196	single nucleotide variant	NM_003565.4(ULK1):c.1027G>A (p.Asp343Asn)	not specified [RCV004195935]	uncertain significance	12	131912020	131912020	Human		name
156186490	CV2346611	single nucleotide variant	NM_003565.4(ULK1):c.2225G>A (p.Arg742His)	not specified [RCV004199639]	uncertain significance	12	131917453	131917453	Human		name
156106476	CV2355250	single nucleotide variant	NM_003565.4(ULK1):c.2309G>A (p.Arg770His)	not specified [RCV004203103]	uncertain significance	12	131917537	131917537	Human		name
155928777	CV2363355	single nucleotide variant	NM_003565.4(ULK1):c.1540C>T (p.Arg514Trp)	not specified [RCV004213898]	uncertain significance	12	131915352	131915352	Human		name
156251260	CV2368777	single nucleotide variant	NM_003565.4(ULK1):c.2089C>T (p.Arg697Cys)	not specified [RCV004214653]	uncertain significance	12	131916969	131916969	Human		name
156268240	CV2371987	single nucleotide variant	NM_003565.4(ULK1):c.1178C>T (p.Ala393Val)	not specified [RCV004221663]	uncertain significance	12	131913767	131913767	Human		name
156080195	CV2384604	single nucleotide variant	NM_003565.4(ULK1):c.1078G>A (p.Val360Ile)	not specified [RCV004232388]	uncertain significance	12	131912071	131912071	Human		name
329377716	CV2436011	single nucleotide variant	NM_003565.4(ULK1):c.2092C>T (p.Leu698Phe)	not specified [RCV004255231]	uncertain significance	12	131916972	131916972	Human		name
329366737	CV2441852	single nucleotide variant	NM_003565.4(ULK1):c.1259C>T (p.Pro420Leu)	not specified [RCV004262048]	uncertain significance	12	131914363	131914363	Human		name
329391586	CV2448732	single nucleotide variant	NM_003565.4(ULK1):c.2594G>A (p.Gly865Asp)	not specified [RCV004259387]	uncertain significance	12	131919294	131919294	Human		name
329376775	CV2455062	single nucleotide variant	NM_003565.4(ULK1):c.2107C>A (p.Leu703Ile)	not specified [RCV004272313]	uncertain significance	12	131916987	131916987	Human		name
329351964	CV2455537	single nucleotide variant	NM_003565.4(ULK1):c.2842G>T (p.Val948Leu)	not specified [RCV004276795]	uncertain significance	12	131920017	131920017	Human		name
401726992	CV2684422	single nucleotide variant	NM_003565.4(ULK1):c.2690C>A (p.Ala897Glu)	not specified [RCV004291498]	uncertain significance	12	131919477	131919477	Human		name
401729241	CV2690111	single nucleotide variant	NM_003565.4(ULK1):c.2218G>A (p.Gly740Arg)	not specified [RCV004300343]	uncertain significance	12	131917446	131917446	Human		name
401744717	CV2697057	single nucleotide variant	NM_003565.4(ULK1):c.1852C>T (p.Pro618Ser)	not specified [RCV004293042]	uncertain significance	12	131916133	131916133	Human		name
401758404	CV2704490	single nucleotide variant	NM_003565.4(ULK1):c.1252G>A (p.Ala418Thr)	not specified [RCV004313232]	uncertain significance	12	131914356	131914356	Human		name
401734329	CV2709457	single nucleotide variant	NM_003565.4(ULK1):c.1912A>T (p.Ser638Cys)	not specified [RCV004318705]	uncertain significance	12	131916431	131916431	Human		name
401862664	CV2762312	single nucleotide variant	NM_003565.4(ULK1):c.2726T>A (p.Leu909Gln)	not specified [RCV004335428]	uncertain significance	12	131919513	131919513	Human		name
401856082	CV2764332	single nucleotide variant	NM_003565.4(ULK1):c.2690C>T (p.Ala897Val)	not specified [RCV004338905]	uncertain significance	12	131919477	131919477	Human		name
401872842	CV2764364	single nucleotide variant	NM_003565.4(ULK1):c.2411C>G (p.Ala804Gly)	not specified [RCV004338937]	uncertain significance	12	131918581	131918581	Human		name
401887223	CV2775769	single nucleotide variant	NM_003565.4(ULK1):c.1724C>T (p.Thr575Met)	not specified [RCV004350892]	uncertain significance	12	131916005	131916005	Human		name
401864411	CV2777832	single nucleotide variant	NM_003565.4(ULK1):c.1942C>T (p.Arg648Trp)	not specified [RCV004346020]	uncertain significance	12	131916461	131916461	Human		name
405260318	CV3209139	single nucleotide variant	NM_003565.4(ULK1):c.2284G>A (p.Gly762Arg)	ULK1-related disorder [RCV003943844]	likely benign	12	131917512	131917512	Human		name , trait , alternate_id
405805428	CV3348194	single nucleotide variant	NM_003565.4(ULK1):c.1025G>A (p.Arg342Gln)	not specified [RCV004479715]	uncertain significance	12	131912018	131912018	Human		name
405805433	CV3348196	single nucleotide variant	NM_003565.4(ULK1):c.1279G>A (p.Gly427Ser)	not specified [RCV004479717]	uncertain significance	12	131914383	131914383	Human		name
405805435	CV3348197	single nucleotide variant	NM_003565.4(ULK1):c.1486C>G (p.Leu496Val)	not specified [RCV004479718]	uncertain significance	12	131915195	131915195	Human		name
405805437	CV3348198	single nucleotide variant	NM_003565.4(ULK1):c.1541G>A (p.Arg514Gln)	not specified [RCV004479719]	uncertain significance	12	131915353	131915353	Human		name
405805442	CV3348200	single nucleotide variant	NM_003565.4(ULK1):c.1700G>A (p.Arg567His)	not specified [RCV004479721]	uncertain significance	12	131915981	131915981	Human		name
405805444	CV3348201	single nucleotide variant	NM_003565.4(ULK1):c.1807C>T (p.Arg603Trp)	not specified [RCV004479722]	uncertain significance	12	131916088	131916088	Human		name
405805446	CV3348202	single nucleotide variant	NM_003565.4(ULK1):c.2033G>A (p.Gly678Asp)	not specified [RCV004479723]	uncertain significance	12	131916552	131916552	Human		name
405805448	CV3348203	single nucleotide variant	NM_003565.4(ULK1):c.2039G>A (p.Arg680Gln)	not specified [RCV004479724]	uncertain significance	12	131916558	131916558	Human		name
405805450	CV3348204	single nucleotide variant	NM_003565.4(ULK1):c.2084C>G (p.Thr695Ser)	not specified [RCV004479725]	uncertain significance	12	131916964	131916964	Human		name
405805452	CV3348205	single nucleotide variant	NM_003565.4(ULK1):c.2117C>T (p.Ala706Val)	not specified [RCV004479726]	uncertain significance	12	131916997	131916997	Human		name
405805455	CV3348206	single nucleotide variant	NM_003565.4(ULK1):c.2183C>T (p.Ala728Val)	not specified [RCV004479727]	uncertain significance	12	131917411	131917411	Human		name
405805457	CV3348207	single nucleotide variant	NM_003565.4(ULK1):c.2201G>C (p.Gly734Ala)	not specified [RCV004479728]	uncertain significance	12	131917429	131917429	Human		name
405805459	CV3348208	single nucleotide variant	NM_003565.4(ULK1):c.2228C>A (p.Ala743Asp)	not specified [RCV004479729]	uncertain significance	12	131917456	131917456	Human		name
405805461	CV3348209	single nucleotide variant	NM_003565.4(ULK1):c.2344G>T (p.Ala782Ser)	not specified [RCV004479730]	uncertain significance	12	131918514	131918514	Human		name
405805466	CV3348211	single nucleotide variant	NM_003565.4(ULK1):c.2612C>T (p.Ala871Val)	not specified [RCV004479732]	uncertain significance	12	131919312	131919312	Human		name
405805468	CV3348212	single nucleotide variant	NM_003565.4(ULK1):c.2732C>G (p.Ser911Cys)	not specified [RCV004479733]	uncertain significance	12	131919519	131919519	Human		name
405805470	CV3348213	single nucleotide variant	NM_003565.4(ULK1):c.2867G>A (p.Arg956Gln)	not specified [RCV004479734]	uncertain significance	12	131920042	131920042	Human		name
407523418	CV3489195	single nucleotide variant	NM_003565.4(ULK1):c.1037G>C (p.Gly346Ala)	not specified [RCV004678080]	uncertain significance	12	131912030	131912030	Human		name
407523488	CV3489196	single nucleotide variant	NM_003565.4(ULK1):c.2279C>A (p.Pro760Gln)	not specified [RCV004678081]	uncertain significance	12	131917507	131917507	Human		name
407523490	CV3489197	single nucleotide variant	NM_003565.4(ULK1):c.2883C>G (p.Phe961Leu)	not specified [RCV004678082]	uncertain significance	12	131920058	131920058	Human		name
407523493	CV3489198	single nucleotide variant	NM_003565.4(ULK1):c.1601C>T (p.Pro534Leu)	not specified [RCV004678083]	uncertain significance	12	131915413	131915413	Human		name
407462458	CV3489200	single nucleotide variant	NM_003565.4(ULK1):c.2297C>T (p.Pro766Leu)	not specified [RCV004687968]	uncertain significance	12	131917525	131917525	Human		name
407523504	CV3489203	single nucleotide variant	NM_003565.4(ULK1):c.1596G>T (p.Arg532Ser)	not specified [RCV004678087]	uncertain significance	12	131915408	131915408	Human		name
407523507	CV3489204	single nucleotide variant	NM_003565.4(ULK1):c.2441C>G (p.Pro814Arg)	not specified [RCV004678088]	uncertain significance	12	131918611	131918611	Human		name
597790031	CV3632605	single nucleotide variant	NM_003565.4(ULK1):c.2221G>A (p.Ala741Thr)	not specified [RCV004876244]	uncertain significance	12	131917449	131917449	Human		name
597790037	CV3632606	single nucleotide variant	NM_003565.4(ULK1):c.1403C>T (p.Thr468Ile)	not specified [RCV004876245]	uncertain significance	12	131915112	131915112	Human		name
597790038	CV3632607	single nucleotide variant	NM_003565.4(ULK1):c.2266G>A (p.Val756Met)	not specified [RCV004876246]	uncertain significance	12	131917494	131917494	Human		name
597790043	CV3632608	single nucleotide variant	NM_003565.4(ULK1):c.1778C>T (p.Ser593Phe)	not specified [RCV004876247]	uncertain significance	12	131916059	131916059	Human		name
597790051	CV3632610	single nucleotide variant	NM_003565.4(ULK1):c.2279C>T (p.Pro760Leu)	not specified [RCV004876249]	uncertain significance	12	131917507	131917507	Human		name
597720383	CV3632612	single nucleotide variant	NM_003565.4(ULK1):c.2360G>A (p.Arg787His)	not specified [RCV004887821]	uncertain significance	12	131918530	131918530	Human		name
597790062	CV3632614	single nucleotide variant	NM_003565.4(ULK1):c.2422G>C (p.Gly808Arg)	not specified [RCV004876252]	uncertain significance	12	131918592	131918592	Human		name
597790066	CV3632615	single nucleotide variant	NM_003565.4(ULK1):c.2174T>G (p.Met725Arg)	not specified [RCV004876253]	uncertain significance	12	131917054	131917054	Human		name
597720395	CV3632616	single nucleotide variant	NM_003565.4(ULK1):c.2593G>A (p.Gly865Ser)	not specified [RCV004887822]	uncertain significance	12	131919293	131919293	Human		name
597790073	CV3632618	single nucleotide variant	NM_003565.4(ULK1):c.2195G>C (p.Gly732Ala)	not specified [RCV004876255]	uncertain significance	12	131917423	131917423	Human		name
597720406	CV3632619	single nucleotide variant	NM_003565.4(ULK1):c.1258C>T (p.Pro420Ser)	not specified [RCV004887823]	uncertain significance	12	131914362	131914362	Human		name
597790081	CV3632622	single nucleotide variant	NM_003565.4(ULK1):c.1803C>A (p.Asn601Lys)	not specified [RCV004876257]	uncertain significance	12	131916084	131916084	Human		name
597790085	CV3632623	single nucleotide variant	NM_003565.4(ULK1):c.2458G>A (p.Glu820Lys)	not specified [RCV004876258]	uncertain significance	12	131918628	131918628	Human		name
597790089	CV3632624	single nucleotide variant	NM_003565.4(ULK1):c.1783G>A (p.Gly595Ser)	not specified [RCV004876259]	uncertain significance	12	131916064	131916064	Human		name
597720417	CV3632625	single nucleotide variant	NM_003565.4(ULK1):c.1589G>C (p.Gly530Ala)	not specified [RCV004887824]	uncertain significance	12	131915401	131915401	Human		name
597720427	CV3632626	single nucleotide variant	NM_003565.4(ULK1):c.1829A>G (p.Asp610Gly)	not specified [RCV004887825]	uncertain significance	12	131916110	131916110	Human		name
597720438	CV3632627	single nucleotide variant	NM_003565.4(ULK1):c.1693G>A (p.Val565Ile)	not specified [RCV004887826]	uncertain significance	12	131915974	131915974	Human		name
597720449	CV3632628	single nucleotide variant	NM_003565.4(ULK1):c.1072G>A (p.Val358Ile)	not specified [RCV004887827]	uncertain significance	12	131912065	131912065	Human		name
597790093	CV3632629	single nucleotide variant	NM_003565.4(ULK1):c.2243G>A (p.Ser748Asn)	not specified [RCV004876260]	uncertain significance	12	131917471	131917471	Human		name
597790096	CV3632630	single nucleotide variant	NM_003565.4(ULK1):c.2329G>A (p.Gly777Ser)	not specified [RCV004876261]	uncertain significance	12	131918499	131918499	Human		name
597790100	CV3632631	single nucleotide variant	NM_003565.4(ULK1):c.1384A>G (p.Ile462Val)	not specified [RCV004876262]	likely benign	12	131915093	131915093	Human		name
598190781	CV3925455	single nucleotide variant	NM_003565.4(ULK1):c.2177A>G (p.Glu726Gly)	not specified [RCV005288257]	uncertain significance	12	131917057	131917057	Human		name
598190788	CV3925456	single nucleotide variant	NM_003565.4(ULK1):c.1253C>T (p.Ala418Val)	not specified [RCV005288258]	uncertain significance	12	131914357	131914357	Human		name
598266418	CV3925457	single nucleotide variant	NM_003565.4(ULK1):c.1337G>A (p.Arg446Gln)	not specified [RCV005301935]	likely benign	12	131914441	131914441	Human		name
598266422	CV3925458	single nucleotide variant	NM_003565.4(ULK1):c.2005C>A (p.Pro669Thr)	not specified [RCV005301936]	uncertain significance	12	131916524	131916524	Human		name
598266426	CV3925459	single nucleotide variant	NM_003565.4(ULK1):c.2140C>G (p.Pro714Ala)	not specified [RCV005301937]	uncertain significance	12	131917020	131917020	Human		name
598190794	CV3925460	single nucleotide variant	NM_003565.4(ULK1):c.2065T>G (p.Phe689Val)	not specified [RCV005288259]	uncertain significance	12	131916584	131916584	Human		name
598190808	CV3925462	single nucleotide variant	NM_003565.4(ULK1):c.1202C>T (p.Thr401Ile)	not specified [RCV005288261]	uncertain significance	12	131913791	131913791	Human		name
598266431	CV3925463	single nucleotide variant	NM_003565.4(ULK1):c.2252C>T (p.Pro751Leu)	not specified [RCV005301938]	uncertain significance	12	131917480	131917480	Human		name
598266435	CV3925464	single nucleotide variant	NM_003565.4(ULK1):c.1979C>T (p.Thr660Met)	not specified [RCV005301939]	uncertain significance	12	131916498	131916498	Human		name
598266439	CV3925465	single nucleotide variant	NM_003565.4(ULK1):c.1282G>A (p.Ala428Thr)	not specified [RCV005301940]	uncertain significance	12	131914386	131914386	Human		name
598190817	CV3925466	single nucleotide variant	NM_003565.4(ULK1):c.2765G>A (p.Arg922Gln)	not specified [RCV005288262]	uncertain significance	12	131919552	131919552	Human		name
598266443	CV3925467	single nucleotide variant	NM_003565.4(ULK1):c.1948G>A (p.Gly650Ser)	not specified [RCV005301941]	uncertain significance	12	131916467	131916467	Human		name
598266448	CV3925468	single nucleotide variant	NM_003565.4(ULK1):c.1265C>G (p.Ser422Cys)	not specified [RCV005301942]	uncertain significance	12	131914369	131914369	Human		name
15127827	CV717942	single nucleotide variant	NM_003565.4(ULK1):c.1355C>G (p.Thr452Ser)	not provided [RCV000963975]	benign	12	131914459	131914459	Human	2	name
15127827	CV717942	single nucleotide variant	NM_003565.4(ULK1):c.1355C>G (p.Thr452Ser)	not provided [RCV000963975]	benign	12	131914459	131914460	Human	2	name
15155063	CV717943	single nucleotide variant	NM_003565.4(ULK1):c.1994C>T (p.Ser665Leu)	not provided [RCV000968855]	benign	12	131916513	131916513	Human		name
15176566	CV743548	single nucleotide variant	NM_003565.4(ULK1):c.1721C>G (p.Pro574Arg)	ULK1-related disorder [RCV003932912]\|not provided [RCV000906458]	likely benign	12	131916002	131916002	Human		name , trait , alternate_id
8627226	CV82370	single nucleotide variant	NM_003565.2(ULK1):c.1631C>G (p.Ser544Cys)	Malignant melanoma [RCV000062449]	not provided	12	131915912	131915912	Human		name
405805472	CV3348214	single nucleotide variant	NM_003565.4(ULK1):c.3010G>A (p.Val1004Ile)	not specified [RCV004479735]	uncertain significance	12	131921148	131921148	Human		name
405805474	CV3348215	single nucleotide variant	NM_003565.4(ULK1):c.3065C>T (p.Ser1022Leu)	not specified [RCV004479736]	uncertain significance	12	131921203	131921203	Human		name
597790054	CV3632611	single nucleotide variant	NM_003565.4(ULK1):c.3034C>A (p.Leu1012Met)	not specified [RCV004876250]	uncertain significance	12	131921172	131921172	Human		name
597790077	CV3632621	single nucleotide variant	NM_003565.4(ULK1):c.3017G>A (p.Arg1006His)	not specified [RCV004876256]	uncertain significance	12	131921155	131921155	Human		name

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