Eml5 Variant Search Result - Rat Genome Database

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159 records found for search term Eml5

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
12896137	CV390526	duplication	NM_183387.3(EML5):c.5203-9dup	not specified [RCV000454930]	benign	14	88620934	88620935	Human		name
8584112	CV118683	single nucleotide variant	NM_183387.2(EML5):c.198-4036T>A	Lung cancer [RCV000099203]	uncertain significance	14	88758707	88758707	Human		name
8584113	CV118684	single nucleotide variant	NM_183387.2(EML5):c.198-16005C>G	Lung cancer [RCV000099204]	uncertain significance	14	88770676	88770676	Human		name
407507058	CV3434984	single nucleotide variant	NM_183387.3(EML5):c.29A>G (p.His10Arg)	not specified [RCV004624959]	uncertain significance	14	88792475	88792475	Human		name
597747423	CV3667824	single nucleotide variant	NM_183387.3(EML5):c.77A>G (p.Asn26Ser)	not specified [RCV004922864]	uncertain significance	14	88792427	88792427	Human		name
597685363	CV3667846	single nucleotide variant	NM_183387.3(EML5):c.64C>T (p.His22Tyr)	not specified [RCV004914775]	uncertain significance	14	88792440	88792440	Human		name
329354216	CV2437003	single nucleotide variant	NM_183387.3(EML5):c.286C>A (p.Gln96Lys)	not specified [RCV004260370]	uncertain significance	14	88754583	88754583	Human		name
405755391	CV3248912	single nucleotide variant	NM_183387.3(EML5):c.241G>A (p.Val81Ile)	not specified [RCV004382599]	uncertain significance	14	88754628	88754628	Human		name
597747443	CV3667817	single nucleotide variant	NM_183387.3(EML5):c.292A>G (p.Ile98Val)	not specified [RCV004922860]	likely benign	14	88754577	88754577	Human		name
597685251	CV3667829	single nucleotide variant	NM_183387.3(EML5):c.101A>G (p.Lys34Arg)	not specified [RCV004914763]	uncertain significance	14	88792403	88792403	Human		name
597685261	CV3667832	single nucleotide variant	NM_183387.3(EML5):c.245G>A (p.Gly82Glu)	not specified [RCV004914764]	uncertain significance	14	88754624	88754624	Human		name
156094939	CV2252992	single nucleotide variant	NM_183387.3(EML5):c.733G>A (p.Ala245Thr)	not specified [RCV004120798]	uncertain significance	14	88738993	88738993	Human		name
401902137	CV2810626	single nucleotide variant	NM_183387.3(EML5):c.4812C>T (p.Ile1604=)	not provided [RCV003393545]	likely benign	14	88625056	88625056	Human		name
401902139	CV2810627	single nucleotide variant	NM_183387.3(EML5):c.3387C>A (p.Thr1129=)	not provided [RCV003393546]	likely benign	14	88664515	88664515	Human		name
405755419	CV3248916	single nucleotide variant	NM_183387.3(EML5):c.395T>C (p.Val132Ala)	not specified [RCV004382603]	uncertain significance	14	88746246	88746246	Human		name
405755527	CV3248931	single nucleotide variant	NM_183387.3(EML5):c.710C>T (p.Ala237Val)	not specified [RCV004382618]	uncertain significance	14	88740388	88740388	Human		name
405755533	CV3248932	single nucleotide variant	NM_183387.3(EML5):c.881A>G (p.Asp294Gly)	not specified [RCV004382619]	uncertain significance	14	88736532	88736532	Human		name
405755539	CV3248933	single nucleotide variant	NM_183387.3(EML5):c.898A>G (p.Thr300Ala)	not specified [RCV004382620]	uncertain significance	14	88736515	88736515	Human		name
407507054	CV3434982	single nucleotide variant	NM_183387.3(EML5):c.676A>G (p.Ile226Val)	not specified [RCV004624957]	uncertain significance	14	88740422	88740422	Human		name
597747448	CV3667814	single nucleotide variant	NM_183387.3(EML5):c.680A>G (p.Asn227Ser)	not specified [RCV004922859]	uncertain significance	14	88740418	88740418	Human		name
597685203	CV3667821	single nucleotide variant	NM_183387.3(EML5):c.893T>C (p.Val298Ala)	not specified [RCV004914758]	uncertain significance	14	88736520	88736520	Human		name
597685222	CV3667825	single nucleotide variant	NM_183387.3(EML5):c.826G>A (p.Glu276Lys)	not specified [RCV004914760]	uncertain significance	14	88738900	88738900	Human		name
597685265	CV3667833	single nucleotide variant	NM_183387.3(EML5):c.359G>A (p.Arg120His)	not specified [RCV004914765]	uncertain significance	14	88746282	88746282	Human		name
598192680	CV3958023	single nucleotide variant	NM_183387.3(EML5):c.854C>T (p.Ser285Phe)	not specified [RCV005335042]	uncertain significance	14	88736559	88736559	Human		name
598192707	CV3958028	single nucleotide variant	NM_183387.3(EML5):c.649A>G (p.Asn217Asp)	not specified [RCV005335047]	uncertain significance	14	88740449	88740449	Human		name
15187273	CV703012	single nucleotide variant	NM_183387.3(EML5):c.4083A>G (p.Val1361=)	not provided [RCV000953538]	benign	14	88644457	88644457	Human		name
15173509	CV703013	single nucleotide variant	NM_183387.3(EML5):c.581C>T (p.Thr194Met)	not provided [RCV000950231]	benign	14	88740517	88740517	Human		name
8635318	CV90540	single nucleotide variant	NM_183387.2(EML5):c.4914A>G (p.Gly1638=)	Malignant melanoma [RCV000070638]	not provided	14	88622703	88622703	Human		name
8635319	CV90541	single nucleotide variant	NM_183387.2(EML5):c.673G>A (p.Gly225Arg)	Malignant melanoma [RCV000070639]	not provided	14	88740425	88740425	Human		name
156369500	CV2193999	single nucleotide variant	NM_183387.3(EML5):c.2698A>G (p.Lys900Glu)	not specified [RCV004074720]	uncertain significance	14	88688315	88688315	Human		name
156397651	CV2197369	single nucleotide variant	NM_183387.3(EML5):c.1133G>A (p.Gly378Glu)	not specified [RCV004081111]	uncertain significance	14	88726595	88726595	Human		name
156138334	CV2202814	single nucleotide variant	NM_183387.3(EML5):c.1709G>A (p.Arg570Lys)	not specified [RCV004073672]	uncertain significance	14	88706375	88706375	Human		name
156280044	CV2252206	single nucleotide variant	NM_183387.3(EML5):c.2702C>T (p.Ala901Val)	not specified [RCV004122212]	uncertain significance	14	88688311	88688311	Human		name
156370002	CV2263456	single nucleotide variant	NM_183387.3(EML5):c.1043C>T (p.Ser348Leu)	not specified [RCV004133701]	uncertain significance	14	88736370	88736370	Human		name
156336305	CV2270681	single nucleotide variant	NM_183387.3(EML5):c.1844A>G (p.His615Arg)	not specified [RCV004137890]	uncertain significance	14	88705570	88705570	Human		name
156260287	CV2274175	single nucleotide variant	NM_183387.3(EML5):c.1984A>C (p.Lys662Gln)	not specified [RCV004134809]	uncertain significance	14	88704927	88704927	Human		name
155994911	CV2278023	single nucleotide variant	NM_183387.3(EML5):c.2906G>A (p.Gly969Asp)	not specified [RCV004141253]	uncertain significance	14	88685091	88685091	Human		name
156080134	CV2292666	single nucleotide variant	NM_183387.3(EML5):c.2470A>G (p.Met824Val)	not specified [RCV004154352]	uncertain significance	14	88694376	88694376	Human		name
156169893	CV2317108	single nucleotide variant	NM_183387.3(EML5):c.1411G>A (p.Gly471Arg)	not specified [RCV004174588]	uncertain significance	14	88714972	88714972	Human		name
155977415	CV2338762	single nucleotide variant	NM_183387.3(EML5):c.2589T>A (p.Asn863Lys)	not specified [RCV004182325]	uncertain significance	14	88688424	88688424	Human		name
329393113	CV2449503	single nucleotide variant	NM_183387.3(EML5):c.2633C>T (p.Ala878Val)	not specified [RCV004268441]	uncertain significance	14	88688380	88688380	Human		name
329378063	CV2461064	single nucleotide variant	NM_183387.3(EML5):c.2554G>A (p.Gly852Arg)	not specified [RCV004265211]	uncertain significance	14	88688459	88688459	Human		name
401728767	CV2673040	single nucleotide variant	NM_183387.3(EML5):c.1843C>T (p.His615Tyr)	not specified [RCV004284032]	uncertain significance	14	88705571	88705571	Human		name
401720736	CV2702082	single nucleotide variant	NM_183387.3(EML5):c.2848T>C (p.Ser950Pro)	not specified [RCV004320654]	uncertain significance	14	88687222	88687222	Human		name
401750092	CV2704979	single nucleotide variant	NM_183387.3(EML5):c.2933G>A (p.Gly978Asp)	not specified [RCV004309586]	uncertain significance	14	88685064	88685064	Human		name
401763236	CV2720244	single nucleotide variant	NM_183387.3(EML5):c.1673A>G (p.Lys558Arg)	not specified [RCV004325577]	uncertain significance	14	88706411	88706411	Human		name
401883400	CV2761086	single nucleotide variant	NM_183387.3(EML5):c.1967A>G (p.Gln656Arg)	not specified [RCV004338745]	uncertain significance	14	88704944	88704944	Human		name
401895804	CV2775683	single nucleotide variant	NM_183387.3(EML5):c.1402A>G (p.Thr468Ala)	not specified [RCV004350818]	uncertain significance	14	88714981	88714981	Human		name
405755307	CV3248901	single nucleotide variant	NM_183387.3(EML5):c.1307G>C (p.Gly436Ala)	not specified [RCV004382588]	uncertain significance	14	88715076	88715076	Human		name
405755315	CV3248902	single nucleotide variant	NM_183387.3(EML5):c.1392A>C (p.Arg464Ser)	not specified [RCV004382589]	uncertain significance	14	88714991	88714991	Human		name
405755321	CV3248903	single nucleotide variant	NM_183387.3(EML5):c.1465A>T (p.Thr489Ser)	not specified [RCV004382590]	uncertain significance	14	88712463	88712463	Human		name
405755331	CV3248904	single nucleotide variant	NM_183387.3(EML5):c.1556A>G (p.Asn519Ser)	not specified [RCV004382591]	uncertain significance	14	88712372	88712372	Human		name
405755337	CV3248905	single nucleotide variant	NM_183387.3(EML5):c.1558G>T (p.Asp520Tyr)	not specified [RCV004382592]	uncertain significance	14	88712370	88712370	Human		name
405755344	CV3248906	single nucleotide variant	NM_183387.3(EML5):c.1570G>T (p.Val524Leu)	not specified [RCV004382593]	uncertain significance	14	88712358	88712358	Human		name
405755354	CV3248907	single nucleotide variant	NM_183387.3(EML5):c.1648T>G (p.Leu550Val)	not specified [RCV004382594]	uncertain significance	14	88712280	88712280	Human		name
405755363	CV3248908	single nucleotide variant	NM_183387.3(EML5):c.1757A>G (p.His586Arg)	not specified [RCV004382595]	uncertain significance	14	88706327	88706327	Human		name
405755369	CV3248909	single nucleotide variant	NM_183387.3(EML5):c.1834G>A (p.Ala612Thr)	not specified [RCV004382596]	uncertain significance	14	88705580	88705580	Human		name
405755375	CV3248910	single nucleotide variant	NM_183387.3(EML5):c.1990G>T (p.Ala664Ser)	not specified [RCV004382597]	uncertain significance	14	88704921	88704921	Human		name
405755382	CV3248911	single nucleotide variant	NM_183387.3(EML5):c.2026A>C (p.Ser676Arg)	not specified [RCV004382598]	uncertain significance	14	88704885	88704885	Human		name
407507050	CV3434979	single nucleotide variant	NM_183387.3(EML5):c.1184T>A (p.Val395Glu)	not specified [RCV004624954]	uncertain significance	14	88726544	88726544	Human		name
407507062	CV3434986	single nucleotide variant	NM_183387.3(EML5):c.2203A>G (p.Ile735Val)	not specified [RCV004624961]	uncertain significance	14	88702481	88702481	Human		name
407507065	CV3434988	single nucleotide variant	NM_183387.3(EML5):c.2205T>G (p.Ile735Met)	not specified [RCV004624963]	uncertain significance	14	88702479	88702479	Human		name
597685193	CV3667819	single nucleotide variant	NM_183387.3(EML5):c.1696G>A (p.Val566Ile)	not specified [RCV004914757]	uncertain significance	14	88706388	88706388	Human		name
597685213	CV3667822	single nucleotide variant	NM_183387.3(EML5):c.1480G>A (p.Gly494Ser)	not specified [RCV004914759]	uncertain significance	14	88712448	88712448	Human		name
597685234	CV3667827	single nucleotide variant	NM_183387.3(EML5):c.1078A>G (p.Ile360Val)	not specified [RCV004914761]	uncertain significance	14	88726650	88726650	Human		name
597685298	CV3667838	single nucleotide variant	NM_183387.3(EML5):c.1465A>G (p.Thr489Ala)	not specified [RCV004914768]	uncertain significance	14	88712463	88712463	Human		name
597685317	CV3667840	single nucleotide variant	NM_183387.3(EML5):c.2092C>G (p.Gln698Glu)	not specified [RCV004914770]	uncertain significance	14	88702592	88702592	Human		name
597685327	CV3667841	single nucleotide variant	NM_183387.3(EML5):c.1330G>A (p.Val444Ile)	not specified [RCV004914771]	uncertain significance	14	88715053	88715053	Human		name
597685344	CV3667844	single nucleotide variant	NM_183387.3(EML5):c.1658G>C (p.Gly553Ala)	not specified [RCV004914773]	uncertain significance	14	88706426	88706426	Human		name
597685354	CV3667845	single nucleotide variant	NM_183387.3(EML5):c.1993A>G (p.Thr665Ala)	not specified [RCV004914774]	uncertain significance	14	88704918	88704918	Human		name
597747389	CV3667847	single nucleotide variant	NM_183387.3(EML5):c.2672G>T (p.Arg891Ile)	not specified [RCV004922871]	uncertain significance	14	88688341	88688341	Human		name
598192597	CV3958007	single nucleotide variant	NM_183387.3(EML5):c.2480A>G (p.Tyr827Cys)	not specified [RCV005335026]	uncertain significance	14	88694366	88694366	Human		name
598192616	CV3958011	single nucleotide variant	NM_183387.3(EML5):c.1819C>T (p.Pro607Ser)	not specified [RCV005335030]	uncertain significance	14	88706265	88706265	Human		name
598192622	CV3958012	single nucleotide variant	NM_183387.3(EML5):c.1999A>G (p.Lys667Glu)	not specified [RCV005335031]	uncertain significance	14	88704912	88704912	Human		name
598192628	CV3958013	single nucleotide variant	NM_183387.3(EML5):c.1844A>T (p.His615Leu)	not specified [RCV005335032]	uncertain significance	14	88705570	88705570	Human		name
598192633	CV3958014	single nucleotide variant	NM_183387.3(EML5):c.2530C>T (p.Arg844Cys)	not specified [RCV005335033]	uncertain significance	14	88694316	88694316	Human		name
598192638	CV3958015	single nucleotide variant	NM_183387.3(EML5):c.1109G>A (p.Arg370His)	not specified [RCV005335034]	uncertain significance	14	88726619	88726619	Human		name
598192643	CV3958016	single nucleotide variant	NM_183387.3(EML5):c.2369T>C (p.Val790Ala)	not specified [RCV005335035]	uncertain significance	14	88695430	88695430	Human		name
598192648	CV3958017	single nucleotide variant	NM_183387.3(EML5):c.1422A>C (p.Lys474Asn)	not specified [RCV005335036]	uncertain significance	14	88714961	88714961	Human		name
598192653	CV3958018	single nucleotide variant	NM_183387.3(EML5):c.1229C>A (p.Ala410Glu)	not specified [RCV005335037]	uncertain significance	14	88715154	88715154	Human		name
598192673	CV3958022	single nucleotide variant	NM_183387.3(EML5):c.1069C>A (p.His357Asn)	not specified [RCV005335041]	uncertain significance	14	88726659	88726659	Human		name
598192686	CV3958024	single nucleotide variant	NM_183387.3(EML5):c.1228G>C (p.Ala410Pro)	not specified [RCV005335043]	uncertain significance	14	88715155	88715155	Human		name
598192697	CV3958026	single nucleotide variant	NM_183387.3(EML5):c.2296A>G (p.Ile766Val)	not specified [RCV005335045]	uncertain significance	14	88696895	88696895	Human		name
598192702	CV3958027	single nucleotide variant	NM_183387.3(EML5):c.1486C>G (p.His496Asp)	not specified [RCV005335046]	uncertain significance	14	88712442	88712442	Human		name
598192712	CV3958029	single nucleotide variant	NM_183387.3(EML5):c.2263A>T (p.Ile755Leu)	not specified [RCV005335048]	uncertain significance	14	88696928	88696928	Human		name
598192733	CV3958033	single nucleotide variant	NM_183387.3(EML5):c.2621C>T (p.Thr874Ile)	not specified [RCV005335052]	uncertain significance	14	88688392	88688392	Human		name
598192741	CV3958034	single nucleotide variant	NM_183387.3(EML5):c.2475C>A (p.Asn825Lys)	not specified [RCV005335053]	uncertain significance	14	88694371	88694371	Human		name
598192746	CV3958035	single nucleotide variant	NM_183387.3(EML5):c.2858T>C (p.Leu953Pro)	not specified [RCV005335054]	uncertain significance	14	88685139	88685139	Human		name
598192757	CV3958037	single nucleotide variant	NM_183387.3(EML5):c.2632G>A (p.Ala878Thr)	not specified [RCV005335056]	uncertain significance	14	88688381	88688381	Human		name
156387869	CV2221638	single nucleotide variant	NM_183387.3(EML5):c.3021C>A (p.His1007Gln)	not specified [RCV004096886]	uncertain significance	14	88681993	88681993	Human		name
156184712	CV2222530	single nucleotide variant	NM_183387.3(EML5):c.3892G>A (p.Val1298Ile)	not specified [RCV004099369]	uncertain significance	14	88657488	88657488	Human		name
156181926	CV2255154	single nucleotide variant	NM_183387.3(EML5):c.5417A>G (p.Glu1806Gly)	not specified [RCV004115777]	uncertain significance	14	88618771	88618771	Human		name
156193401	CV2296965	single nucleotide variant	NM_183387.3(EML5):c.4555G>A (p.Gly1519Ser)	not specified [RCV004150897]	uncertain significance	14	88627023	88627023	Human		name
156072889	CV2299122	single nucleotide variant	NM_183387.3(EML5):c.4844C>T (p.Ala1615Val)	not specified [RCV004152475]	uncertain significance	14	88625024	88625024	Human		name
156189563	CV2302961	single nucleotide variant	NM_183387.3(EML5):c.5468T>C (p.Ile1823Thr)	not specified [RCV004162836]	uncertain significance	14	88618720	88618720	Human		name
156169102	CV2315432	single nucleotide variant	NM_183387.3(EML5):c.3424G>A (p.Val1142Ile)	not specified [RCV004167389]	uncertain significance	14	88663105	88663105	Human		name
155907738	CV2354489	single nucleotide variant	NM_183387.3(EML5):c.4706G>A (p.Arg1569Gln)	not specified [RCV004202476]	uncertain significance	14	88626872	88626872	Human		name
156010305	CV2362107	single nucleotide variant	NM_183387.3(EML5):c.3946C>T (p.Arg1316Cys)	not specified [RCV004209912]	uncertain significance	14	88657434	88657434	Human		name
155910270	CV2369811	single nucleotide variant	NM_183387.3(EML5):c.3733C>T (p.Arg1245Cys)	not specified [RCV004215198]	uncertain significance	14	88658331	88658331	Human		name
156141603	CV2383707	single nucleotide variant	NM_183387.3(EML5):c.5597T>C (p.Met1866Thr)	not specified [RCV004231595]	uncertain significance	14	88618273	88618273	Human		name
156057254	CV2396327	single nucleotide variant	NM_183387.3(EML5):c.5570A>G (p.Tyr1857Cys)	not specified [RCV004242056]	uncertain significance	14	88618300	88618300	Human		name
329400460	CV2438354	single nucleotide variant	NM_183387.3(EML5):c.3123G>T (p.Lys1041Asn)	not specified [RCV004259516]	uncertain significance	14	88681891	88681891	Human		name
401738252	CV2676180	single nucleotide variant	NM_183387.3(EML5):c.4694T>A (p.Leu1565Gln)	not specified [RCV004284398]	uncertain significance	14	88626884	88626884	Human		name
401779574	CV2676617	single nucleotide variant	NM_183387.3(EML5):c.3209A>G (p.Asp1070Gly)	not specified [RCV004282577]	uncertain significance	14	88665405	88665405	Human		name
401738120	CV2700987	single nucleotide variant	NM_183387.3(EML5):c.4539A>C (p.Lys1513Asn)	not specified [RCV004307242]	uncertain significance	14	88627039	88627039	Human		name
401730446	CV2711311	single nucleotide variant	NM_183387.3(EML5):c.3952A>G (p.Met1318Val)	not specified [RCV004313085]	uncertain significance	14	88657428	88657428	Human		name
401733334	CV2713054	single nucleotide variant	NM_183387.3(EML5):c.4261C>T (p.His1421Tyr)	not specified [RCV004316613]	uncertain significance	14	88638884	88638884	Human		name
401770104	CV2719038	single nucleotide variant	NM_183387.3(EML5):c.4746C>G (p.Asn1582Lys)	not specified [RCV004322620]	uncertain significance	14	88625122	88625122	Human		name
401784106	CV2721048	single nucleotide variant	NM_183387.3(EML5):c.3368G>C (p.Gly1123Ala)	not specified [RCV004328317]	uncertain significance	14	88664534	88664534	Human		name
401762256	CV2723375	single nucleotide variant	NM_183387.3(EML5):c.3821G>A (p.Arg1274Gln)	not specified [RCV004329583]	uncertain significance	14	88658243	88658243	Human		name
401736786	CV2725233	single nucleotide variant	NM_183387.3(EML5):c.5449G>C (p.Gly1817Arg)	not specified [RCV004321748]	uncertain significance	14	88618739	88618739	Human		name
401770627	CV2726209	single nucleotide variant	NM_183387.3(EML5):c.3433G>A (p.Gly1145Ser)	not specified [RCV004326678]	uncertain significance	14	88663096	88663096	Human		name
401764833	CV2728099	single nucleotide variant	NM_183387.3(EML5):c.5624C>G (p.Thr1875Ser)	not specified [RCV004324196]	uncertain significance	14	88618246	88618246	Human		name
401718171	CV2728460	single nucleotide variant	NM_183387.3(EML5):c.3994A>G (p.Ile1332Val)	not specified [RCV004333430]	likely benign	14	88657386	88657386	Human		name
401884648	CV2761883	single nucleotide variant	NM_183387.3(EML5):c.5588A>G (p.Lys1863Arg)	not specified [RCV004339522]	uncertain significance	14	88618282	88618282	Human		name
401889861	CV2763469	single nucleotide variant	NM_183387.3(EML5):c.3169G>A (p.Val1057Ile)	not specified [RCV004349353]	uncertain significance	14	88665445	88665445	Human		name
401874382	CV2773929	single nucleotide variant	NM_183387.3(EML5):c.4993C>T (p.Arg1665Cys)	not specified [RCV004358354]	uncertain significance	14	88622624	88622624	Human		name
401898572	CV2784680	single nucleotide variant	NM_183387.3(EML5):c.3576A>C (p.Glu1192Asp)	not specified [RCV004352497]	uncertain significance	14	88661753	88661753	Human		name
405755407	CV3248914	single nucleotide variant	NM_183387.3(EML5):c.3196A>G (p.Met1066Val)	not specified [RCV004382601]	uncertain significance	14	88665418	88665418	Human		name
405755412	CV3248915	single nucleotide variant	NM_183387.3(EML5):c.3562C>A (p.Pro1188Thr)	not specified [RCV004382602]	uncertain significance	14	88661767	88661767	Human		name
405755428	CV3248917	single nucleotide variant	NM_183387.3(EML5):c.4169A>G (p.Tyr1390Cys)	not specified [RCV004382604]	uncertain significance	14	88642961	88642961	Human		name
405755433	CV3248918	single nucleotide variant	NM_183387.3(EML5):c.4366C>A (p.Pro1456Thr)	not specified [RCV004382605]	uncertain significance	14	88627811	88627811	Human		name
405755442	CV3248919	single nucleotide variant	NM_183387.3(EML5):c.4723G>A (p.Ala1575Thr)	not specified [RCV004382606]	uncertain significance	14	88626855	88626855	Human		name
405755449	CV3248920	single nucleotide variant	NM_183387.3(EML5):c.4817C>T (p.Ala1606Val)	not specified [RCV004382607]	uncertain significance	14	88625051	88625051	Human		name
405755454	CV3248921	single nucleotide variant	NM_183387.3(EML5):c.4846A>C (p.Met1616Leu)	not specified [RCV004382608]	uncertain significance	14	88625022	88625022	Human		name
405755460	CV3248922	single nucleotide variant	NM_183387.3(EML5):c.4952G>A (p.Arg1651His)	not specified [RCV004382609]	uncertain significance	14	88622665	88622665	Human		name
405755465	CV3248923	single nucleotide variant	NM_183387.3(EML5):c.5019G>T (p.Lys1673Asn)	not specified [RCV004382610]	uncertain significance	14	88621296	88621296	Human		name
405755472	CV3248924	single nucleotide variant	NM_183387.3(EML5):c.5174C>T (p.Thr1725Ile)	not specified [RCV004382611]	uncertain significance	14	88621141	88621141	Human		name
405755479	CV3248925	single nucleotide variant	NM_183387.3(EML5):c.5207T>C (p.Met1736Thr)	not specified [RCV004382612]	uncertain significance	14	88620922	88620922	Human		name
405755486	CV3248926	single nucleotide variant	NM_183387.3(EML5):c.5237C>T (p.Ala1746Val)	not specified [RCV004382613]	uncertain significance	14	88620892	88620892	Human		name
405755491	CV3248927	single nucleotide variant	NM_183387.3(EML5):c.5495T>C (p.Phe1832Ser)	not specified [RCV004382614]	uncertain significance	14	88618693	88618693	Human		name
405755499	CV3248928	single nucleotide variant	NM_183387.3(EML5):c.5561G>T (p.Arg1854Leu)	not specified [RCV004382615]	uncertain significance	14	88618309	88618309	Human		name
405755510	CV3248929	single nucleotide variant	NM_183387.3(EML5):c.5807A>T (p.Lys1936Ile)	not specified [RCV004382616]	uncertain significance	14	88616232	88616232	Human		name
405755517	CV3248930	single nucleotide variant	NM_183387.3(EML5):c.5911A>G (p.Lys1971Glu)	not specified [RCV004382617]	uncertain significance	14	88615841	88615841	Human		name
407507047	CV3434978	single nucleotide variant	NM_183387.3(EML5):c.4103T>C (p.Ile1368Thr)	not specified [RCV004624953]	uncertain significance	14	88644437	88644437	Human		name
407479244	CV3434981	single nucleotide variant	NM_183387.3(EML5):c.5272G>C (p.Val1758Leu)	not specified [RCV004624956]	uncertain significance	14	88620857	88620857	Human		name
407479248	CV3434983	single nucleotide variant	NM_183387.3(EML5):c.5887G>A (p.Asp1963Asn)	not specified [RCV004624958]	uncertain significance	14	88616152	88616152	Human		name
407507060	CV3434985	single nucleotide variant	NM_183387.3(EML5):c.3338T>G (p.Met1113Arg)	not specified [RCV004624960]	uncertain significance	14	88664564	88664564	Human		name
407479252	CV3434987	single nucleotide variant	NM_183387.3(EML5):c.4751C>T (p.Thr1584Met)	not specified [RCV004624962]	uncertain significance	14	88625117	88625117	Human		name
597685172	CV3667815	single nucleotide variant	NM_183387.3(EML5):c.5212A>C (p.Asn1738His)	not specified [RCV004914755]	uncertain significance	14	88620917	88620917	Human		name
597685731	CV3667816	single nucleotide variant	NM_183387.3(EML5):c.3947G>A (p.Arg1316His)	not specified [RCV004914756]	uncertain significance	14	88657433	88657433	Human		name
597747438	CV3667818	single nucleotide variant	NM_183387.3(EML5):c.5926C>T (p.Pro1976Ser)	not specified [RCV004922861]	uncertain significance	14	88615826	88615826	Human		name
597747428	CV3667823	single nucleotide variant	NM_183387.3(EML5):c.3085C>G (p.Pro1029Ala)	not specified [RCV004922863]	uncertain significance	14	88681929	88681929	Human		name
597747417	CV3667826	single nucleotide variant	NM_183387.3(EML5):c.4646C>A (p.Thr1549Asn)	not specified [RCV004922865]	uncertain significance	14	88626932	88626932	Human		name
597685244	CV3667828	single nucleotide variant	NM_183387.3(EML5):c.4644G>C (p.Trp1548Cys)	not specified [RCV004914762]	uncertain significance	14	88626934	88626934	Human		name
597747413	CV3667830	single nucleotide variant	NM_183387.3(EML5):c.5576T>C (p.Val1859Ala)	not specified [RCV004922866]	uncertain significance	14	88618294	88618294	Human		name
597747403	CV3667834	single nucleotide variant	NM_183387.3(EML5):c.5843T>C (p.Ile1948Thr)	not specified [RCV004922868]	uncertain significance	14	88616196	88616196	Human		name
597685276	CV3667835	single nucleotide variant	NM_183387.3(EML5):c.4427A>G (p.His1476Arg)	not specified [RCV004914766]	uncertain significance	14	88627750	88627750	Human		name
597685287	CV3667836	single nucleotide variant	NM_183387.3(EML5):c.4862G>A (p.Arg1621Gln)	not specified [RCV004914767]	uncertain significance	14	88625006	88625006	Human		name
597747399	CV3667837	single nucleotide variant	NM_183387.3(EML5):c.3314G>A (p.Ser1105Asn)	not specified [RCV004922869]	uncertain significance	14	88664588	88664588	Human		name
597685308	CV3667839	single nucleotide variant	NM_183387.3(EML5):c.4048C>T (p.Pro1350Ser)	not specified [RCV004914769]	uncertain significance	14	88644492	88644492	Human		name
598192611	CV3958010	single nucleotide variant	NM_183387.3(EML5):c.3954G>C (p.Met1318Ile)	not specified [RCV005335029]	uncertain significance	14	88657426	88657426	Human		name
598192662	CV3958020	single nucleotide variant	NM_183387.3(EML5):c.5252A>G (p.Tyr1751Cys)	not specified [RCV005335039]	uncertain significance	14	88620877	88620877	Human		name
598192667	CV3958021	single nucleotide variant	NM_183387.3(EML5):c.3493G>C (p.Val1165Leu)	not specified [RCV005335040]	uncertain significance	14	88663036	88663036	Human		name
598192691	CV3958025	single nucleotide variant	NM_183387.3(EML5):c.4907A>G (p.Glu1636Gly)	not specified [RCV005335044]	uncertain significance	14	88622710	88622710	Human		name
598192722	CV3958031	single nucleotide variant	NM_183387.3(EML5):c.4562A>G (p.Asn1521Ser)	not specified [RCV005335050]	uncertain significance	14	88627016	88627016	Human		name
598192728	CV3958032	single nucleotide variant	NM_183387.3(EML5):c.4255C>G (p.Gln1419Glu)	not specified [RCV005335051]	uncertain significance	14	88638890	88638890	Human		name
598192752	CV3958036	single nucleotide variant	NM_183387.3(EML5):c.3251T>C (p.Met1084Thr)	not specified [RCV005335055]	uncertain significance	14	88665363	88665363	Human		name
15156672	CV725850	single nucleotide variant	NM_183387.3(EML5):c.5360C>A (p.Ala1787Glu)	not provided [RCV000880677]	benign	14	88620769	88620769	Human		name

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