Ros1 Variant Search Result - Rat Genome Database

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242 records found for search term Ros1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15200001	CV730387	single nucleotide variant	NM_001378902.1(ROS1):c.883+3A>G	not provided [RCV000890792]	benign	6	117396185	117396185	Human		name
15117197	CV779154	duplication	NM_001378902.1(ROS1):c.883+8dup	not provided [RCV000962162]	benign	6	117396179	117396180	Human		name
596946907	CV3546964	single nucleotide variant	NM_001378902.1(ROS1):c.3840-5T>C	not provided [RCV004810770]	benign	6	117356920	117356920	Human		name
598128787	CV3886585	single nucleotide variant	NM_001378902.1(ROS1):c.5923-4A>G	not provided [RCV005244245]	benign	6	117318256	117318256	Human		name
617151493	CV4022003	single nucleotide variant	NM_001378902.1(ROS1):c.5759+4T>G	not provided [RCV005426964]	benign	6	117321255	117321255	Human		name
15151568	CV730386	single nucleotide variant	NM_001378902.1(ROS1):c.4126+3A>G	not provided [RCV000879623]	likely benign	6	117356626	117356626	Human		name
15106236	CV759421	single nucleotide variant	NM_001378902.1(ROS1):c.1191+8C>T	not provided [RCV000915707]	benign	6	117394154	117394154	Human		name
15138122	CV779180	single nucleotide variant	NM_001378902.1(ROS1):c.5348+9G>A	not provided [RCV000965735]	benign	6	117329320	117329320	Human		name
15169826	CV779186	single nucleotide variant	NM_001378902.1(ROS1):c.2583-3C>T	not provided [RCV000971890]	benign	6	117366293	117366293	Human		name
243053373	CV2404573	single nucleotide variant	NM_001378902.1(ROS1):c.3430+42C>T	Lung adenocarcinoma [RCV003129600]	benign	6	117360300	117360300	Human	2	name
243053706	CV2404634	single nucleotide variant	NM_001378902.1(ROS1):c.5062-46A>C	Lung adenocarcinoma [RCV003129661]	uncertain significance	6	117337386	117337386	Human	2	name
243053616	CV2404691	single nucleotide variant	NM_001378902.1(ROS1):c.3366+23T>C	Squamous cell carcinoma [RCV003129718]	uncertain significance	6	117362580	117362580	Human	2	name
617151490	CV4022004	single nucleotide variant	NM_001378902.1(ROS1):c.5540-26T>A	not provided [RCV005426965]	benign	6	117324441	117324441	Human		name
401920886	CV2820658	single nucleotide variant	NM_001378902.1(ROS1):c.5760-265G>T	not provided [RCV003432020]	benign	6	117320295	117320295	Human		name
15195495	CV765447	single nucleotide variant	NM_001378902.1(ROS1):c.60A>G (p.Leu20=)	not provided [RCV000933954]	likely benign	6	117425597	117425597	Human		name
405718991	CV3309812	single nucleotide variant	NM_001378902.1(ROS1):c.26C>T (p.Pro9Leu)	not specified [RCV004449560]	likely benign	6	117425631	117425631	Human		name
15152998	CV710142	single nucleotide variant	NM_001378902.1(ROS1):c.264G>A (p.Ser88=)	not provided [RCV000968461]	benign\|likely benign	6	117409634	117409634	Human		name
8626079	CV81223	single nucleotide variant	NM_002944.2(ROS1):c.6294G>A (p.Val2098=)	Malignant melanoma [RCV000061301]	not provided	6	117310221	117310221	Human		name
597756155	CV3586997	single nucleotide variant	NM_001378902.1(ROS1):c.61T>C (p.Trp21Arg)	not specified [RCV004847734]	uncertain significance	6	117425596	117425596	Human		name
15104301	CV699278	single nucleotide variant	NM_001378902.1(ROS1):c.666C>T (p.Val222=)	not provided [RCV000959657]	benign	6	117397055	117397055	Human		name
8626081	CV81225	single nucleotide variant	NM_002944.2(ROS1):c.2651C>T (p.Ser884Phe)	Malignant melanoma [RCV000061303]	not provided	6	117366237	117366237	Human		name
8631791	CV86997	single nucleotide variant	NM_002944.2(ROS1):c.1742C>T (p.Ala581Val)	Malignant melanoma [RCV000067088]	not provided	6	117389367	117389367	Human		name
8631792	CV86998	single nucleotide variant	NM_002944.2(ROS1):c.1333G>A (p.Glu445Lys)	Malignant melanoma [RCV000067089]	not provided	6	117389776	117389776	Human		name
155905122	CV2349683	single nucleotide variant	NM_001378902.1(ROS1):c.267T>G (p.Cys89Trp)	not specified [RCV004204099]	uncertain significance	6	117409631	117409631	Human		name
401777961	CV2718400	single nucleotide variant	NM_001378902.1(ROS1):c.139C>T (p.Leu47Phe)	not specified [RCV004318225]	uncertain significance	6	117418491	117418491	Human		name
405286580	CV3192239	single nucleotide variant	NM_001378902.1(ROS1):c.2796A>C (p.Pro932=)	ROS1-related disorder [RCV003924141]	likely benign	6	117366077	117366077	Human		name , trait , alternate_id
597756176	CV3586984	single nucleotide variant	NM_001378902.1(ROS1):c.186C>G (p.His62Gln)	not specified [RCV004847729]	uncertain significance	6	117416300	117416300	Human		name
617153041	CV4021015	single nucleotide variant	NM_001378902.1(ROS1):c.2778A>G (p.Thr926=)	not provided [RCV005428768]	likely benign	6	117366095	117366095	Human		name
15172558	CV710140	single nucleotide variant	NM_001378902.1(ROS1):c.2004T>C (p.Ser668=)	not provided [RCV000972429]	benign	6	117386995	117386995	Human		name
15192661	CV721686	single nucleotide variant	NM_001378902.1(ROS1):c.2151G>A (p.Thr717=)	not provided [RCV000888724]	benign	6	117385821	117385821	Human		name
8626080	CV81224	single nucleotide variant	NM_002944.2(ROS1):c.3586G>A (p.Gly1196Arg)	Malignant melanoma [RCV000061302]	not provided	6	117359871	117359871	Human		name
150529844	CV1289238	single nucleotide variant	NM_001378902.1(ROS1):c.706G>A (p.Gly236Ser)	not specified [RCV001728070]	uncertain significance	6	117397015	117397015	Human		name
156235072	CV2193364	single nucleotide variant	NM_001378902.1(ROS1):c.736C>A (p.Gln246Lys)	not specified [RCV004072867]	uncertain significance	6	117396985	117396985	Human		name
156295143	CV2233703	single nucleotide variant	NM_001378902.1(ROS1):c.631A>C (p.Asn211His)	not specified [RCV004100150]	uncertain significance	6	117397090	117397090	Human		name
156033442	CV2275122	single nucleotide variant	NM_001378902.1(ROS1):c.779A>G (p.Tyr260Cys)	not specified [RCV004136925]	uncertain significance	6	117396942	117396942	Human		name
155922957	CV2340710	single nucleotide variant	NM_001378902.1(ROS1):c.895G>C (p.Glu299Gln)	not specified [RCV004190381]	uncertain significance	6	117394727	117394727	Human		name
156339860	CV2351657	single nucleotide variant	NM_001378902.1(ROS1):c.994C>A (p.His332Asn)	not specified [RCV004195369]	uncertain significance	6	117394628	117394628	Human		name
243053572	CV2404658	single nucleotide variant	NM_001378902.1(ROS1):c.682C>G (p.Gln228Glu)	Lung adenocarcinoma [RCV003129685]	uncertain significance	6	117397039	117397039	Human	2	name
401899008	CV2785939	single nucleotide variant	NM_001378902.1(ROS1):c.884T>C (p.Val295Ala)	not specified [RCV004359785]	uncertain significance	6	117394738	117394738	Human		name
401920884	CV2820657	single nucleotide variant	NM_001378902.1(ROS1):c.6369T>C (p.Ala2123=)	not provided [RCV003432019]	likely benign	6	117310128	117310128	Human		name
401915960	CV2820660	single nucleotide variant	NM_001378902.1(ROS1):c.3543C>T (p.Ala1181=)	not provided [RCV003428932]	likely benign	6	117359899	117359899	Human		name
405719031	CV3309817	single nucleotide variant	NM_001378902.1(ROS1):c.391G>A (p.Ala131Thr)	not specified [RCV004449565]	uncertain significance	6	117404354	117404354	Human		name
405719105	CV3309825	single nucleotide variant	NM_001378902.1(ROS1):c.485A>G (p.Tyr162Cys)	not specified [RCV004449573]	uncertain significance	6	117403258	117403258	Human		name
405719267	CV3309843	single nucleotide variant	NM_001378902.1(ROS1):c.976C>T (p.Arg326Trp)	not specified [RCV004449591]	uncertain significance	6	117394646	117394646	Human		name
407487231	CV3479906	single nucleotide variant	NM_001378902.1(ROS1):c.738A>C (p.Gln246His)	not specified [RCV004665627]	uncertain significance	6	117396983	117396983	Human		name
407487251	CV3479912	single nucleotide variant	NM_001378902.1(ROS1):c.875C>T (p.Ser292Phe)	not specified [RCV004665631]	uncertain significance	6	117396196	117396196	Human		name
596946932	CV3546989	single nucleotide variant	NM_001378902.1(ROS1):c.527G>A (p.Arg176Gln)	not provided [RCV004810795]	benign	6	117403216	117403216	Human		name
597689432	CV3586974	single nucleotide variant	NM_001378902.1(ROS1):c.985G>A (p.Ala329Thr)	not specified [RCV004858704]	uncertain significance	6	117394637	117394637	Human		name
597708473	CV3586981	single nucleotide variant	NM_001378902.1(ROS1):c.752G>C (p.Gly251Ala)	not specified [RCV004860729]	uncertain significance	6	117396969	117396969	Human		name
597756167	CV3586989	single nucleotide variant	NM_001378902.1(ROS1):c.755C>G (p.Thr252Arg)	not specified [RCV004847731]	uncertain significance	6	117396966	117396966	Human		name
597708520	CV3586992	single nucleotide variant	NM_001378902.1(ROS1):c.662A>G (p.Glu221Gly)	not specified [RCV004860735]	uncertain significance	6	117397059	117397059	Human		name
597708537	CV3586994	single nucleotide variant	NM_001378902.1(ROS1):c.368A>C (p.Asn123Thr)	not specified [RCV004860737]	uncertain significance	6	117404377	117404377	Human		name
598128786	CV3886584	single nucleotide variant	NM_001378902.1(ROS1):c.6229A>C (p.Arg2077=)	not provided [RCV005244244]	benign	6	117310268	117310268	Human		name
598128806	CV3886604	single nucleotide variant	NM_001378902.1(ROS1):c.5724C>T (p.Ala1908=)	not provided [RCV005244264]	benign	6	117321294	117321294	Human		name
598217870	CV3906154	single nucleotide variant	NM_001378902.1(ROS1):c.634A>G (p.Ile212Val)	not specified [RCV005272137]	uncertain significance	6	117397087	117397087	Human		name
617153022	CV4020747	single nucleotide variant	NM_001378902.1(ROS1):c.4765T>C (p.Leu1589=)	not provided [RCV005428500]	benign	6	117341519	117341519	Human		name
15177632	CV699273	single nucleotide variant	NM_001378902.1(ROS1):c.5076G>A (p.Glu1692=)	not provided [RCV000951088]	likely benign	6	117337326	117337326	Human		name
15100832	CV699275	single nucleotide variant	NM_001378902.1(ROS1):c.4401A>C (p.Thr1467=)	not provided [RCV000958974]	benign	6	117344165	117344165	Human		name
15197229	CV699276	single nucleotide variant	NM_001378902.1(ROS1):c.3516G>A (p.Thr1172=)	not provided [RCV000956408]	benign	6	117359926	117359926	Human		name
15184483	CV710137	single nucleotide variant	NM_001378902.1(ROS1):c.3375C>A (p.Ala1125=)	not provided [RCV000975123]	benign	6	117360397	117360397	Human		name
15176973	CV721684	single nucleotide variant	NM_001378902.1(ROS1):c.6246C>T (p.Ser2082=)	not provided [RCV000884713]	likely benign	6	117310251	117310251	Human		name
15151387	CV721688	single nucleotide variant	NM_001378902.1(ROS1):c.697C>T (p.Pro233Ser)	not provided [RCV000879585]	benign	6	117397024	117397024	Human		name
15154809	CV735380	single nucleotide variant	NM_001378902.1(ROS1):c.5202C>T (p.Thr1734=)	not provided [RCV000902024]	likely benign	6	117337200	117337200	Human		name
15168553	CV735381	single nucleotide variant	NM_001378902.1(ROS1):c.3894T>C (p.Ser1298=)	not provided [RCV000904879]	benign\|likely benign	6	117356861	117356861	Human		name
15185779	CV735385	single nucleotide variant	NM_001378902.1(ROS1):c.451T>C (p.Trp151Arg)	not provided [RCV000908623]	likely benign	6	117404294	117404294	Human		name
15153678	CV749778	single nucleotide variant	NM_001378902.1(ROS1):c.4035A>G (p.Pro1345=)	not provided [RCV000924105]	likely benign	6	117356720	117356720	Human		name
15100014	CV749779	single nucleotide variant	NM_001378902.1(ROS1):c.3991T>C (p.Leu1331=)	not provided [RCV000914542]	benign	6	117356764	117356764	Human		name
15203256	CV749780	single nucleotide variant	NM_001378902.1(ROS1):c.3675A>C (p.Thr1225=)	not provided [RCV000913812]	likely benign	6	117357968	117357968	Human		name
15182124	CV765446	single nucleotide variant	NM_001378902.1(ROS1):c.4968T>C (p.Pro1656=)	not provided [RCV000930290]	likely benign	6	117341228	117341228	Human		name
156253537	CV2193082	single nucleotide variant	NM_001378902.1(ROS1):c.2425C>G (p.Leu809Val)	not specified [RCV004069626]	uncertain significance	6	117383373	117383373	Human		name
156387114	CV2221407	single nucleotide variant	NM_001378902.1(ROS1):c.2308T>G (p.Leu770Val)	not specified [RCV004096702]	uncertain significance	6	117383490	117383490	Human		name
156130217	CV2238599	single nucleotide variant	NM_001378902.1(ROS1):c.1940G>A (p.Ser647Asn)	not specified [RCV004107207]	uncertain significance	6	117387839	117387839	Human		name
156018439	CV2263189	single nucleotide variant	NM_001378902.1(ROS1):c.2329G>T (p.Val777Phe)	not specified [RCV004131419]	uncertain significance	6	117383469	117383469	Human		name
156277918	CV2330876	single nucleotide variant	NM_001378902.1(ROS1):c.2176C>A (p.Leu726Met)	not specified [RCV004185931]	uncertain significance	6	117385796	117385796	Human		name
156172023	CV2337565	single nucleotide variant	NM_001378902.1(ROS1):c.1460T>C (p.Met487Thr)	not specified [RCV004187989]	uncertain significance	6	117389676	117389676	Human		name
156146849	CV2357963	single nucleotide variant	NM_001378902.1(ROS1):c.2573G>A (p.Arg858Gln)	not specified [RCV004209743]	uncertain significance	6	117379068	117379068	Human		name
156046312	CV2385283	single nucleotide variant	NM_001378902.1(ROS1):c.2375T>C (p.Val792Ala)	not specified [RCV004230569]	uncertain significance	6	117383423	117383423	Human		name
156003110	CV2396693	single nucleotide variant	NM_001378902.1(ROS1):c.2674T>C (p.Trp892Arg)	not specified [RCV004233849]	uncertain significance	6	117366199	117366199	Human		name
329367662	CV2427495	single nucleotide variant	NM_001378902.1(ROS1):c.2665C>T (p.Arg889Trp)	not specified [RCV004250134]	uncertain significance	6	117366208	117366208	Human		name
401749979	CV2695896	single nucleotide variant	NM_001378902.1(ROS1):c.1132A>G (p.Ile378Val)	not specified [RCV004308173]	uncertain significance	6	117394221	117394221	Human		name
401780739	CV2727541	single nucleotide variant	NM_001378902.1(ROS1):c.1676C>T (p.Ser559Leu)	not specified [RCV004329733]	uncertain significance	6	117389460	117389460	Human		name
401889573	CV2756547	single nucleotide variant	NM_001378902.1(ROS1):c.2711T>C (p.Ile904Thr)	not specified [RCV004345074]	uncertain significance	6	117366162	117366162	Human		name
401868472	CV2767246	single nucleotide variant	NM_001378902.1(ROS1):c.1717C>G (p.Leu573Val)	not specified [RCV004349421]	uncertain significance	6	117389419	117389419	Human		name
401887030	CV2777061	single nucleotide variant	NM_001378902.1(ROS1):c.1019A>T (p.Asp340Val)	not specified [RCV004351852]	uncertain significance	6	117394334	117394334	Human		name
401897282	CV2789922	single nucleotide variant	NM_001378902.1(ROS1):c.2929T>C (p.Tyr977His)	not specified [RCV004362300]	uncertain significance	6	117365610	117365610	Human		name
401920889	CV2820661	single nucleotide variant	NM_001378902.1(ROS1):c.2962T>G (p.Leu988Val)	not provided [RCV003432022]	uncertain significance	6	117365201	117365201	Human		name
405717633	CV2851998	duplication	NM_001378902.1(ROS1):c.5588dup (p.Ile1864fs)	Male infertility with azoospermia or oligozoospermia due to single gene mutation [RCV003991626]	likely pathogenic	6	117324366	117324367	Human	1	name
405259803	CV3195244	single nucleotide variant	NM_001378902.1(ROS1):c.1181T>C (p.Met394Thr)	ROS1-related disorder [RCV003894439]	likely benign	6	117394172	117394172	Human		name , trait , alternate_id
405276932	CV3198711	single nucleotide variant	NM_001378902.1(ROS1):c.1135T>C (p.Ser379Pro)	ROS1-related disorder [RCV003904036]	likely benign	6	117394218	117394218	Human		name , trait , alternate_id
405718916	CV3309804	single nucleotide variant	NM_001378902.1(ROS1):c.1352G>A (p.Arg451Gln)	not specified [RCV004449552]	likely benign	6	117389784	117389784	Human		name
405718927	CV3309805	single nucleotide variant	NM_001378902.1(ROS1):c.1723G>A (p.Val575Met)	not specified [RCV004449553]	uncertain significance	6	117389413	117389413	Human		name
405718937	CV3309806	single nucleotide variant	NM_001378902.1(ROS1):c.1736C>T (p.Ser579Phe)	not specified [RCV004449554]	uncertain significance	6	117389400	117389400	Human		name
405718949	CV3309807	single nucleotide variant	NM_001378902.1(ROS1):c.2053C>A (p.Pro685Thr)	not specified [RCV004449555]	uncertain significance	6	117386946	117386946	Human		name
405718959	CV3309808	single nucleotide variant	NM_001378902.1(ROS1):c.2312C>T (p.Thr771Met)	not specified [RCV004449556]	uncertain significance	6	117383486	117383486	Human		name
405718969	CV3309809	single nucleotide variant	NM_001378902.1(ROS1):c.2419A>G (p.Thr807Ala)	not specified [RCV004449557]	uncertain significance	6	117383379	117383379	Human		name
405718975	CV3309810	single nucleotide variant	NM_001378902.1(ROS1):c.2522A>G (p.Tyr841Cys)	not specified [RCV004449558]	uncertain significance	6	117379119	117379119	Human		name
405718986	CV3309811	single nucleotide variant	NM_001378902.1(ROS1):c.2579A>G (p.Gln860Arg)	not specified [RCV004449559]	uncertain significance	6	117379062	117379062	Human		name
405718999	CV3309813	single nucleotide variant	NM_001378902.1(ROS1):c.2777C>T (p.Thr926Ile)	not specified [RCV004449561]	uncertain significance	6	117366096	117366096	Human		name
405719006	CV3309814	single nucleotide variant	NM_001378902.1(ROS1):c.2804T>C (p.Phe935Ser)	not specified [RCV004449562]	uncertain significance	6	117365735	117365735	Human		name
407487228	CV3479905	single nucleotide variant	NM_001378902.1(ROS1):c.2071C>G (p.Pro691Ala)	not specified [RCV004665626]	uncertain significance	6	117386928	117386928	Human		name
407513571	CV3479911	single nucleotide variant	NM_001378902.1(ROS1):c.2857A>G (p.Ile953Val)	not specified [RCV004674174]	uncertain significance	6	117365682	117365682	Human		name
597756207	CV3586970	single nucleotide variant	NM_001378902.1(ROS1):c.2217C>G (p.Ser739Arg)	not specified [RCV004847722]	uncertain significance	6	117385755	117385755	Human		name
597756185	CV3586980	single nucleotide variant	NM_001378902.1(ROS1):c.2806T>C (p.Ser936Pro)	not specified [RCV004847727]	uncertain significance	6	117365733	117365733	Human		name
597756172	CV3586987	single nucleotide variant	NM_001378902.1(ROS1):c.2657A>T (p.Tyr886Phe)	not specified [RCV004847730]	uncertain significance	6	117366216	117366216	Human		name
597708512	CV3586990	single nucleotide variant	NM_001378902.1(ROS1):c.2495C>A (p.Thr832Asn)	not specified [RCV004860734]	uncertain significance	6	117379146	117379146	Human		name
597756163	CV3586991	single nucleotide variant	NM_001378902.1(ROS1):c.2821G>A (p.Val941Ile)	not specified [RCV004847732]	uncertain significance	6	117365718	117365718	Human		name
597708529	CV3586993	single nucleotide variant	NM_001378902.1(ROS1):c.2141A>G (p.Tyr714Cys)	not specified [RCV004860736]	uncertain significance	6	117385831	117385831	Human		name
12858846	CV389125	single nucleotide variant	NM_001378902.1(ROS1):c.1121G>C (p.Gly374Ala)	Abnormal brain morphology [RCV000454139]\|ROS1-related disorder [RCV003942467]\|not provided [RCV003424002]\|not specified [RCV002248663]	likely pathogenic\|likely benign\|uncertain significance	6	117394232	117394232	Human	1	name , trait , alternate_id
598219586	CV3906137	single nucleotide variant	NM_001378902.1(ROS1):c.2648T>G (p.Leu883Arg)	not specified [RCV005272120]	uncertain significance	6	117366225	117366225	Human		name
598219559	CV3906141	single nucleotide variant	NM_001378902.1(ROS1):c.2114T>C (p.Met705Thr)	not specified [RCV005272124]	uncertain significance	6	117385858	117385858	Human		name
598219553	CV3906142	single nucleotide variant	NM_001378902.1(ROS1):c.1036G>A (p.Val346Ile)	not specified [RCV005272125]	uncertain significance	6	117394317	117394317	Human		name
598219485	CV3906152	single nucleotide variant	NM_001378902.1(ROS1):c.2714G>A (p.Gly905Asp)	not specified [RCV005272135]	uncertain significance	6	117366159	117366159	Human		name
14349968	CV590855	deletion	NM_001378902.1(ROS1):c.4583del (p.Asn1528fs)	Short stature [RCV000736226]	pathogenic	6	117342468	117342468	Human	2	name
15168051	CV710138	single nucleotide variant	NM_001378902.1(ROS1):c.2354A>G (p.Asn785Ser)	not provided [RCV000971532]	benign	6	117383444	117383444	Human		name
15153739	CV710139	single nucleotide variant	NM_001378902.1(ROS1):c.2263C>A (p.Leu755Ile)	not provided [RCV000968602]	likely benign	6	117385709	117385709	Human		name
15172563	CV710141	single nucleotide variant	NM_001378902.1(ROS1):c.1408A>G (p.Lys470Glu)	not provided [RCV000972430]	benign	6	117389728	117389728	Human		name
15164645	CV721685	single nucleotide variant	NM_001378902.1(ROS1):c.2396C>A (p.Thr799Asn)	not provided [RCV000882242]	likely benign	6	117383402	117383402	Human		name
15172895	CV721687	single nucleotide variant	NM_001378902.1(ROS1):c.1943C>T (p.Ser648Phe)	not provided [RCV000883933]	likely benign	6	117387836	117387836	Human		name
15124719	CV735383	single nucleotide variant	NM_001378902.1(ROS1):c.2361G>C (p.Met787Ile)	not provided [RCV000896640]	benign	6	117383437	117383437	Human		name
15127492	CV735384	single nucleotide variant	NM_001378902.1(ROS1):c.1838A>G (p.Asp613Gly)	not provided [RCV000897120]	benign	6	117387941	117387941	Human		name
15199101	CV749782	single nucleotide variant	NM_001378902.1(ROS1):c.2809T>C (p.Phe937Leu)	not provided [RCV000912448]	benign	6	117365730	117365730	Human		name
150529842	CV1289237	single nucleotide variant	NM_001378902.1(ROS1):c.6676G>A (p.Glu2226Lys)	not specified [RCV001728069]	uncertain significance	6	117301013	117301013	Human		name
156172215	CV2194214	single nucleotide variant	NM_001378902.1(ROS1):c.5630A>G (p.His1877Arg)	not specified [RCV004079340]	uncertain significance	6	117321388	117321388	Human		name
156188179	CV2195857	single nucleotide variant	NM_001378902.1(ROS1):c.4016C>A (p.Thr1339Asn)	not specified [RCV004076197]	uncertain significance	6	117356739	117356739	Human		name
156168241	CV2197664	single nucleotide variant	NM_001378902.1(ROS1):c.4558T>C (p.Tyr1520His)	not specified [RCV004074873]	uncertain significance	6	117342493	117342493	Human		name
156114152	CV2208880	single nucleotide variant	NM_001378902.1(ROS1):c.6106C>T (p.Arg2036Trp)	not specified [RCV004085252]	uncertain significance	6	117317154	117317154	Human		name
156380941	CV2219058	single nucleotide variant	NM_001378902.1(ROS1):c.5087T>C (p.Val1696Ala)	not specified [RCV004087225]	uncertain significance	6	117337315	117337315	Human		name
155980141	CV2222979	single nucleotide variant	NM_001378902.1(ROS1):c.3107C>G (p.Pro1036Arg)	not specified [RCV004103571]	uncertain significance	6	117362862	117362862	Human		name
155934905	CV2225446	single nucleotide variant	NM_001378902.1(ROS1):c.7003G>A (p.Gly2335Arg)	not specified [RCV004100845]	uncertain significance	6	117288515	117288515	Human		name
155977066	CV2231772	single nucleotide variant	NM_001378902.1(ROS1):c.4588T>C (p.Tyr1530His)	not specified [RCV004098586]	uncertain significance	6	117342463	117342463	Human		name
156117006	CV2231773	single nucleotide variant	NM_001378902.1(ROS1):c.5276G>C (p.Ser1759Thr)	not specified [RCV004098587]	uncertain significance	6	117329401	117329401	Human		name
155983118	CV2239950	single nucleotide variant	NM_001378902.1(ROS1):c.6596G>T (p.Arg2199Ile)	not specified [RCV004110750]	uncertain significance	6	117301093	117301093	Human		name
156136455	CV2245707	single nucleotide variant	NM_001378902.1(ROS1):c.7012G>A (p.Asp2338Asn)	not specified [RCV004111583]	uncertain significance	6	117288506	117288506	Human		name
156076224	CV2248313	single nucleotide variant	NM_001378902.1(ROS1):c.4899C>G (p.His1633Gln)	not specified [RCV004119472]	uncertain significance	6	117341297	117341297	Human		name
156205913	CV2249911	single nucleotide variant	NM_001378902.1(ROS1):c.3569T>C (p.Met1190Thr)	not specified [RCV004122884]	uncertain significance	6	117359873	117359873	Human		name
155993290	CV2253564	single nucleotide variant	NM_001378902.1(ROS1):c.4260T>G (p.Ser1420Arg)	not specified [RCV004125259]	uncertain significance	6	117353033	117353033	Human		name
155920100	CV2254991	single nucleotide variant	NM_001378902.1(ROS1):c.5891T>A (p.Val1964Asp)	not specified [RCV004117216]	uncertain significance	6	117319899	117319899	Human		name
156001740	CV2257888	single nucleotide variant	NM_001378902.1(ROS1):c.3871G>T (p.Gly1291Cys)	not specified [RCV004129714]	uncertain significance	6	117356884	117356884	Human		name
156366600	CV2269734	single nucleotide variant	NM_001378902.1(ROS1):c.4568A>G (p.Gln1523Arg)	not specified [RCV004126985]	uncertain significance	6	117342483	117342483	Human		name
155926319	CV2284852	single nucleotide variant	NM_001378902.1(ROS1):c.5317T>C (p.Cys1773Arg)	not specified [RCV004143312]	uncertain significance	6	117329360	117329360	Human		name
156084131	CV2289664	single nucleotide variant	NM_001378902.1(ROS1):c.4709T>C (p.Ile1570Thr)	not specified [RCV004148576]	uncertain significance	6	117341575	117341575	Human		name
156185847	CV2292349	single nucleotide variant	NM_001378902.1(ROS1):c.5089A>G (p.Lys1697Glu)	not specified [RCV004150159]	uncertain significance	6	117337313	117337313	Human		name
156396476	CV2326292	single nucleotide variant	NM_001378902.1(ROS1):c.3680A>G (p.Asp1227Gly)	not specified [RCV004180538]	uncertain significance	6	117357963	117357963	Human		name
156289786	CV2333229	single nucleotide variant	NM_001378902.1(ROS1):c.5197A>C (p.Ser1733Arg)	not specified [RCV004196562]	uncertain significance	6	117337205	117337205	Human		name
156055155	CV2343376	single nucleotide variant	NM_001378902.1(ROS1):c.3841C>T (p.Arg1281Cys)	not specified [RCV004197458]	uncertain significance	6	117356914	117356914	Human		name
156057454	CV2343547	single nucleotide variant	NM_001378902.1(ROS1):c.3145A>G (p.Ser1049Gly)	not specified [RCV004190581]	uncertain significance	6	117362824	117362824	Human		name
156175325	CV2374373	single nucleotide variant	NM_001378902.1(ROS1):c.6942A>C (p.Gln2314His)	not specified [RCV004231897]	uncertain significance	6	117288576	117288576	Human		name
156060406	CV2380129	single nucleotide variant	NM_001378902.1(ROS1):c.6934G>A (p.Glu2312Lys)	not specified [RCV004224506]	uncertain significance	6	117288584	117288584	Human		name
156227101	CV2388155	single nucleotide variant	NM_001378902.1(ROS1):c.5893G>A (p.Gly1965Arg)	not specified [RCV004234618]	uncertain significance	6	117319897	117319897	Human		name
156198686	CV2392193	single nucleotide variant	NM_001378902.1(ROS1):c.3163A>G (p.Lys1055Glu)	not specified [RCV004242537]	uncertain significance	6	117362806	117362806	Human		name
155998435	CV2396242	single nucleotide variant	NM_001378902.1(ROS1):c.6641A>T (p.Asn2214Ile)	not specified [RCV004240194]	uncertain significance	6	117301048	117301048	Human		name
156165167	CV2398787	single nucleotide variant	NM_001378902.1(ROS1):c.3544G>A (p.Val1182Ile)	not specified [RCV004243814]	likely benign	6	117359898	117359898	Human		name
243053427	CV2404593	single nucleotide variant	NM_001378902.1(ROS1):c.3388G>A (p.Gly1130Arg)	Lung adenocarcinoma [RCV003129620]	pathogenic	6	117360384	117360384	Human	2	name
243053799	CV2404687	single nucleotide variant	NM_001378902.1(ROS1):c.3167A>G (p.Asn1056Ser)	Lung adenocarcinoma [RCV003129714]	uncertain significance	6	117362802	117362802	Human	2	name
401798330	CV2416793	single nucleotide variant	NM_001378902.1(ROS1):c.6079G>A (p.Asp2027Asn)	Lung sarcomatoid carcinoma [RCV003322643]	uncertain significance	6	117317181	117317181	Human	1	name
329388097	CV2468692	single nucleotide variant	NM_001378902.1(ROS1):c.5030A>G (p.Asn1677Ser)	not specified [RCV004280022]	uncertain significance	6	117341166	117341166	Human		name
329353197	CV2468924	single nucleotide variant	NM_001378902.1(ROS1):c.4193G>T (p.Ser1398Ile)	not specified [RCV004274195]	uncertain significance	6	117353100	117353100	Human		name
401737873	CV2676050	single nucleotide variant	NM_001378902.1(ROS1):c.5326A>C (p.Thr1776Pro)	not specified [RCV004284280]	uncertain significance	6	117329351	117329351	Human		name
401755198	CV2682409	single nucleotide variant	NM_001378902.1(ROS1):c.6752A>G (p.Asp2251Gly)	not specified [RCV004290437]	uncertain significance	6	117288766	117288766	Human		name
401749801	CV2694755	single nucleotide variant	NM_001378902.1(ROS1):c.3248T>C (p.Ile1083Thr)	not specified [RCV004298840]	uncertain significance	6	117362721	117362721	Human		name
401747438	CV2696698	single nucleotide variant	NM_001378902.1(ROS1):c.5949G>T (p.Gln1983His)	not specified [RCV004290677]	uncertain significance	6	117318226	117318226	Human		name
401720305	CV2705815	single nucleotide variant	NM_001378902.1(ROS1):c.6236G>A (p.Cys2079Tyr)	not specified [RCV004320434]	uncertain significance	6	117310261	117310261	Human		name
401762137	CV2714029	single nucleotide variant	NM_001378902.1(ROS1):c.3928C>A (p.Pro1310Thr)	not specified [RCV004315434]	uncertain significance	6	117356827	117356827	Human		name
401725534	CV2721816	single nucleotide variant	NM_001378902.1(ROS1):c.3531A>T (p.Arg1177Ser)	not specified [RCV004326332]	uncertain significance	6	117359911	117359911	Human		name
401723970	CV2725108	single nucleotide variant	NM_001378902.1(ROS1):c.5165G>A (p.Arg1722Lys)	not specified [RCV004319853]	uncertain significance	6	117337237	117337237	Human		name
401780604	CV2727468	single nucleotide variant	NM_001378902.1(ROS1):c.5073T>A (p.Asn1691Lys)	not specified [RCV004329672]	uncertain significance	6	117337329	117337329	Human		name
401878020	CV2760156	single nucleotide variant	NM_001378902.1(ROS1):c.6142G>A (p.Val2048Ile)	not specified [RCV004347338]	uncertain significance	6	117311093	117311093	Human		name
401868215	CV2767172	single nucleotide variant	NM_001378902.1(ROS1):c.3746T>C (p.Val1249Ala)	not specified [RCV004347567]	uncertain significance	6	117357897	117357897	Human		name
401891128	CV2769062	single nucleotide variant	NM_001378902.1(ROS1):c.5290C>G (p.Gln1764Glu)	not specified [RCV004348928]	uncertain significance	6	117329387	117329387	Human		name
401894700	CV2785198	single nucleotide variant	NM_001378902.1(ROS1):c.3616A>G (p.Asn1206Asp)	not specified [RCV004356976]	uncertain significance	6	117359826	117359826	Human		name
401898980	CV2792180	single nucleotide variant	NM_001378902.1(ROS1):c.3298A>C (p.Asn1100His)	not specified [RCV004361389]	uncertain significance	6	117362671	117362671	Human		name
401920887	CV2820659	duplication	NM_001378902.1(ROS1):c.5623+1427_5623+1429dup	not provided [RCV003432021]	benign	6	117322902	117322903	Human		name
401944775	CV2840596	single nucleotide variant	NM_001378902.1(ROS1):c.6621C>A (p.Asp2207Glu)	not provided [RCV003457482]	likely benign	6	117301068	117301068	Human		name
405717642	CV2851999	single nucleotide variant	NM_001378902.1(ROS1):c.3611T>A (p.Leu1204Ter)	Male infertility with azoospermia or oligozoospermia due to single gene mutation [RCV003991627]	likely pathogenic	6	117359831	117359831	Human	1	name
405295079	CV3210932	single nucleotide variant	NM_001378902.1(ROS1):c.6967C>G (p.Pro2323Ala)	ROS1-related disorder [RCV003936946]	likely benign	6	117288551	117288551	Human		name , trait , alternate_id
405719013	CV3309815	single nucleotide variant	NM_001378902.1(ROS1):c.3260G>A (p.Ser1087Asn)	not specified [RCV004449563]	uncertain significance	6	117362709	117362709	Human		name
405719024	CV3309816	single nucleotide variant	NM_001378902.1(ROS1):c.3268A>T (p.Asn1090Tyr)	not specified [RCV004449564]	uncertain significance	6	117362701	117362701	Human		name
405719037	CV3309818	single nucleotide variant	NM_001378902.1(ROS1):c.3882G>A (p.Met1294Ile)	not specified [RCV004449566]	uncertain significance	6	117356873	117356873	Human		name
405719045	CV3309819	single nucleotide variant	NM_001378902.1(ROS1):c.4154A>T (p.Asp1385Val)	not specified [RCV004449567]	uncertain significance	6	117353139	117353139	Human		name
405719057	CV3309820	single nucleotide variant	NM_001378902.1(ROS1):c.4304A>G (p.Asp1435Gly)	not specified [RCV004449568]	uncertain significance	6	117344262	117344262	Human		name
405719071	CV3309821	single nucleotide variant	NM_001378902.1(ROS1):c.4358C>T (p.Ala1453Val)	not specified [RCV004449569]	uncertain significance	6	117344208	117344208	Human		name
405719086	CV3309823	single nucleotide variant	NM_001378902.1(ROS1):c.4547C>A (p.Pro1516Gln)	not specified [RCV004449571]	uncertain significance	6	117342504	117342504	Human		name
405719097	CV3309824	single nucleotide variant	NM_001378902.1(ROS1):c.4553C>T (p.Ser1518Leu)	not specified [RCV004449572]	uncertain significance	6	117342498	117342498	Human		name
405719111	CV3309826	single nucleotide variant	NM_001378902.1(ROS1):c.4646A>C (p.Asn1549Thr)	not specified [RCV004449574]	uncertain significance	6	117342405	117342405	Human		name
405719121	CV3309827	single nucleotide variant	NM_001378902.1(ROS1):c.4931C>T (p.Pro1644Leu)	not specified [RCV004449575]	uncertain significance	6	117341265	117341265	Human		name
405719139	CV3309829	single nucleotide variant	NM_001378902.1(ROS1):c.5083C>G (p.His1695Asp)	not specified [RCV004449577]	uncertain significance	6	117337319	117337319	Human		name
405719153	CV3309830	single nucleotide variant	NM_001378902.1(ROS1):c.5105A>T (p.Gln1702Leu)	not specified [RCV004449578]	uncertain significance	6	117337297	117337297	Human		name
405719162	CV3309831	single nucleotide variant	NM_001378902.1(ROS1):c.5209C>G (p.Pro1737Ala)	not specified [RCV004449579]	uncertain significance	6	117337193	117337193	Human		name
405719170	CV3309832	single nucleotide variant	NM_001378902.1(ROS1):c.5225C>A (p.Thr1742Lys)	not specified [RCV004449580]	uncertain significance	6	117337177	117337177	Human		name
405719188	CV3309834	single nucleotide variant	NM_001378902.1(ROS1):c.5789A>G (p.Asn1930Ser)	not specified [RCV004449582]	likely benign	6	117320001	117320001	Human		name
405719194	CV3309835	single nucleotide variant	NM_001378902.1(ROS1):c.5999A>G (p.His2000Arg)	not specified [RCV004449583]	uncertain significance	6	117317261	117317261	Human		name
405719215	CV3309837	single nucleotide variant	NM_001378902.1(ROS1):c.6081C>A (p.Asp2027Glu)	not specified [RCV004449585]	uncertain significance	6	117317179	117317179	Human		name
405719223	CV3309838	single nucleotide variant	NM_001378902.1(ROS1):c.6298G>T (p.Ala2100Ser)	not specified [RCV004449586]	uncertain significance	6	117310199	117310199	Human		name
405719236	CV3309839	single nucleotide variant	NM_001378902.1(ROS1):c.6470C>G (p.Pro2157Arg)	not specified [RCV004449587]	uncertain significance	6	117308875	117308875	Human		name
405719244	CV3309840	single nucleotide variant	NM_001378902.1(ROS1):c.6718G>A (p.Glu2240Lys)	not specified [RCV004449588]	uncertain significance	6	117288800	117288800	Human		name
405719252	CV3309841	single nucleotide variant	NM_001378902.1(ROS1):c.6729T>G (p.Asp2243Glu)	not specified [RCV004449589]	uncertain significance	6	117288789	117288789	Human		name
407487236	CV3479907	single nucleotide variant	NM_001378902.1(ROS1):c.4690T>C (p.Ser1564Pro)	not specified [RCV004665628]	uncertain significance	6	117341594	117341594	Human		name
407513568	CV3479909	single nucleotide variant	NM_001378902.1(ROS1):c.4895G>A (p.Cys1632Tyr)	not specified [RCV004674173]	uncertain significance	6	117341301	117341301	Human		name
407487245	CV3479910	single nucleotide variant	NM_001378902.1(ROS1):c.3848A>G (p.Tyr1283Cys)	not specified [RCV004665630]	uncertain significance	6	117356907	117356907	Human		name
407487255	CV3479913	single nucleotide variant	NM_001378902.1(ROS1):c.4462G>A (p.Val1488Ile)	not specified [RCV004665632]	uncertain significance	6	117344104	117344104	Human		name
408383319	CV3504975	single nucleotide variant	NM_001378902.1(ROS1):c.3998G>A (p.Gly1333Glu)	ROS1-related disorder [RCV004730508]	uncertain significance	6	117356757	117356757	Human		name , trait , alternate_id
597689412	CV3586971	single nucleotide variant	NM_001378902.1(ROS1):c.4295C>G (p.Pro1432Arg)	not specified [RCV004858702]	uncertain significance	6	117352998	117352998	Human		name
597689423	CV3586972	single nucleotide variant	NM_001378902.1(ROS1):c.5401T>C (p.Phe1801Leu)	not specified [RCV004858703]	uncertain significance	6	117326362	117326362	Human		name
597756203	CV3586973	single nucleotide variant	NM_001378902.1(ROS1):c.5960A>C (p.Glu1987Ala)	not specified [RCV004847723]	uncertain significance	6	117318215	117318215	Human		name
597756198	CV3586975	single nucleotide variant	NM_001378902.1(ROS1):c.3475A>G (p.Ile1159Val)	not specified [RCV004847724]	uncertain significance	6	117359967	117359967	Human		name
597689444	CV3586976	single nucleotide variant	NM_001378902.1(ROS1):c.3308C>T (p.Pro1103Leu)	not specified [RCV004858705]	uncertain significance	6	117362661	117362661	Human		name
597756194	CV3586977	single nucleotide variant	NM_001378902.1(ROS1):c.3154T>C (p.Cys1052Arg)	not specified [RCV004847725]	uncertain significance	6	117362815	117362815	Human		name
597756189	CV3586979	single nucleotide variant	NM_001378902.1(ROS1):c.5569A>G (p.Ile1857Val)	not specified [RCV004847726]	uncertain significance	6	117324386	117324386	Human		name
597756181	CV3586982	single nucleotide variant	NM_001378902.1(ROS1):c.6967C>A (p.Pro2323Thr)	not specified [RCV004847728]	uncertain significance	6	117288551	117288551	Human		name
597708481	CV3586983	single nucleotide variant	NM_001378902.1(ROS1):c.6686A>G (p.Asn2229Ser)	not specified [RCV004860730]	uncertain significance	6	117301003	117301003	Human		name
597708487	CV3586985	single nucleotide variant	NM_001378902.1(ROS1):c.4556C>A (p.Thr1519Lys)	not specified [RCV004860731]	uncertain significance	6	117342495	117342495	Human		name
597708494	CV3586986	single nucleotide variant	NM_001378902.1(ROS1):c.6366G>A (p.Met2122Ile)	not specified [RCV004860732]	uncertain significance	6	117310131	117310131	Human		name
597756159	CV3586995	single nucleotide variant	NM_001378902.1(ROS1):c.5722G>A (p.Ala1908Thr)	not specified [RCV004847733]	uncertain significance	6	117321296	117321296	Human		name
597708548	CV3586996	single nucleotide variant	NM_001378902.1(ROS1):c.4797A>T (p.Glu1599Asp)	not specified [RCV004860738]	uncertain significance	6	117341487	117341487	Human		name
12834394	CV363018	single nucleotide variant	NM_001378902.1(ROS1):c.6076G>A (p.Gly2026Arg)	Lung adenocarcinoma [RCV000418413]	pathogenic\|likely pathogenic	6	117317184	117317184	Human	2	name
598128766	CV3886564	single nucleotide variant	NM_001378902.1(ROS1):c.6619G>A (p.Asp2207Asn)	not provided [RCV005244224]	benign	6	117301070	117301070	Human		name
598128767	CV3886565	single nucleotide variant	NM_001378902.1(ROS1):c.3311C>T (p.Ser1104Leu)	not provided [RCV005244225]	benign	6	117362658	117362658	Human		name
598128781	CV3886579	single nucleotide variant	NM_001378902.1(ROS1):c.6668C>G (p.Ser2223Cys)	not provided [RCV005244239]	benign	6	117301021	117301021	Human		name
598128782	CV3886580	single nucleotide variant	NM_001378902.1(ROS1):c.6664A>C (p.Lys2222Gln)	not provided [RCV005244240]	benign	6	117301025	117301025	Human		name
598219578	CV3906138	single nucleotide variant	NM_001378902.1(ROS1):c.3013C>A (p.Pro1005Thr)	not specified [RCV005272121]	uncertain significance	6	117365150	117365150	Human		name
598219572	CV3906139	single nucleotide variant	NM_001378902.1(ROS1):c.5942C>T (p.Thr1981Ile)	not specified [RCV005272122]	uncertain significance	6	117318233	117318233	Human		name
598219565	CV3906140	single nucleotide variant	NM_001378902.1(ROS1):c.4331A>G (p.Asp1444Gly)	not specified [RCV005272123]	uncertain significance	6	117344235	117344235	Human		name
598219547	CV3906143	single nucleotide variant	NM_001378902.1(ROS1):c.5480C>A (p.Ala1827Glu)	not specified [RCV005272126]	uncertain significance	6	117326283	117326283	Human		name
598219527	CV3906146	single nucleotide variant	NM_001378902.1(ROS1):c.6754A>G (p.Ile2252Val)	not specified [RCV005272129]	likely benign	6	117288764	117288764	Human		name
598219521	CV3906147	single nucleotide variant	NM_001378902.1(ROS1):c.3014C>G (p.Pro1005Arg)	not specified [RCV005272130]	uncertain significance	6	117365149	117365149	Human		name
598219514	CV3906148	single nucleotide variant	NM_001378902.1(ROS1):c.3844T>G (p.Leu1282Val)	not specified [RCV005272131]	uncertain significance	6	117356911	117356911	Human		name
598219507	CV3906149	single nucleotide variant	NM_001378902.1(ROS1):c.3524C>G (p.Ala1175Gly)	not specified [RCV005272132]	uncertain significance	6	117359918	117359918	Human		name
598219501	CV3906150	single nucleotide variant	NM_001378902.1(ROS1):c.3910T>G (p.Leu1304Val)	not specified [RCV005272133]	uncertain significance	6	117356845	117356845	Human		name
598219495	CV3906151	single nucleotide variant	NM_001378902.1(ROS1):c.4669C>T (p.Leu1557Phe)	not specified [RCV005272134]	uncertain significance	6	117341615	117341615	Human		name
598217863	CV3906153	single nucleotide variant	NM_001378902.1(ROS1):c.6785A>G (p.Asn2262Ser)	not specified [RCV005272136]	uncertain significance	6	117288733	117288733	Human		name
598217877	CV3906155	single nucleotide variant	NM_001378902.1(ROS1):c.6830A>G (p.Gln2277Arg)	not specified [RCV005272138]	uncertain significance	6	117288688	117288688	Human		name
14349958	CV590856	single nucleotide variant	NM_001378902.1(ROS1):c.3073A>G (p.Thr1025Ala)	Short stature [RCV000736227]	uncertain significance	6	117365090	117365090	Human	2	name
15170852	CV699271	single nucleotide variant	NM_001378902.1(ROS1):c.5686G>A (p.Glu1896Lys)	not provided [RCV000949726]	benign	6	117321332	117321332	Human		name
15187293	CV699272	single nucleotide variant	NM_001378902.1(ROS1):c.5308G>C (p.Asp1770His)	not provided [RCV000953544]	benign	6	117329369	117329369	Human		name
15197226	CV699274	single nucleotide variant	NM_001378902.1(ROS1):c.4498A>G (p.Arg1500Gly)	not provided [RCV000956407]	benign	6	117344068	117344068	Human		name
15104296	CV699277	single nucleotide variant	NM_001378902.1(ROS1):c.3269A>T (p.Asn1090Ile)	not provided [RCV000959656]	benign\|likely benign	6	117362700	117362700	Human		name
15127256	CV710135	single nucleotide variant	NM_001378902.1(ROS1):c.6965A>G (p.Lys2322Arg)	not provided [RCV000963870]	benign	6	117288553	117288553	Human		name
15122217	CV710136	single nucleotide variant	NM_001378902.1(ROS1):c.4957C>A (p.Pro1653Thr)	not provided [RCV000963035]	benign	6	117341239	117341239	Human		name
15157269	CV721683	single nucleotide variant	NM_001378902.1(ROS1):c.6359G>A (p.Arg2120Gln)	not provided [RCV000880789]	benign\|conflicting interpretations of pathogenicity	6	117310138	117310138	Human		name
15174564	CV735379	single nucleotide variant	NM_001378902.1(ROS1):c.5650A>G (p.Lys1884Glu)	not provided [RCV000905994]	likely benign	6	117321368	117321368	Human		name
15128714	CV735382	single nucleotide variant	NM_001378902.1(ROS1):c.3065G>A (p.Gly1022Asp)	not provided [RCV000897322]	likely benign	6	117365098	117365098	Human		name
15199096	CV749781	single nucleotide variant	NM_001378902.1(ROS1):c.3062A>T (p.Lys1021Met)	not provided [RCV000912447]	benign	6	117365101	117365101	Human		name

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