Neu4 Variant Search Result - Rat Genome Database

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83 records found for search term Neu4

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405712404	CV3350465	single nucleotide variant	NM_001167600.3(NEU4):c.14G>A (p.Arg5His)	not specified [RCV004494039]	likely benign	2	241814498	241814498	Human		name
155906524	CV2357339	single nucleotide variant	NM_001167600.3(NEU4):c.77C>T (p.Ser26Leu)	not specified [RCV004200228]	uncertain significance	2	241814561	241814561	Human		name
155916973	CV2366796	single nucleotide variant	NM_001167600.3(NEU4):c.70G>A (p.Val24Met)	not specified [RCV004210786]	uncertain significance	2	241814554	241814554	Human		name
401879293	CV2791365	single nucleotide variant	NM_001167600.3(NEU4):c.67C>T (p.Arg23Cys)	not specified [RCV004358771]	uncertain significance	2	241814551	241814551	Human		name
401919562	CV2827015	single nucleotide variant	NM_001167600.3(NEU4):c.450C>T (p.Ala150=)	not provided [RCV003431218]	likely benign	2	241815140	241815140	Human		name
401930435	CV2827016	single nucleotide variant	NM_001167600.3(NEU4):c.840C>T (p.Ile280=)	not provided [RCV003440300]	likely benign	2	241816433	241816433	Human		name
407526490	CV3451047	single nucleotide variant	NM_001167600.3(NEU4):c.50G>A (p.Arg17Lys)	not specified [RCV004654830]	uncertain significance	2	241814534	241814534	Human		name
407526499	CV3451050	single nucleotide variant	NM_001167600.3(NEU4):c.88G>A (p.Val30Met)	not specified [RCV004654833]	uncertain significance	2	241814572	241814572	Human		name
597639959	CV3565707	single nucleotide variant	NM_001167600.3(NEU4):c.85C>T (p.Pro29Ser)	not specified [RCV004832020]	uncertain significance	2	241814569	241814569	Human		name
598254747	CV4000531	single nucleotide variant	NM_001167600.3(NEU4):c.47A>G (p.Glu16Gly)	not specified [RCV005385544]	uncertain significance	2	241814531	241814531	Human		name
156326578	CV2219639	single nucleotide variant	NM_001167600.3(NEU4):c.103A>C (p.Thr35Pro)	not specified [RCV004093748]	uncertain significance	2	241814587	241814587	Human		name
156334967	CV2333459	single nucleotide variant	NM_001167600.3(NEU4):c.265C>T (p.Pro89Ser)	not specified [RCV004190160]	uncertain significance	2	241814955	241814955	Human		name
156146695	CV2357954	single nucleotide variant	NM_001167600.3(NEU4):c.217G>A (p.Val73Met)	not specified [RCV004209736]	uncertain significance	2	241814907	241814907	Human		name
405712213	CV3350438	single nucleotide variant	NM_001167600.3(NEU4):c.125A>G (p.Gln42Arg)	not specified [RCV004494012]	uncertain significance	2	241814609	241814609	Human		name
407526506	CV3451052	single nucleotide variant	NM_001167600.3(NEU4):c.259C>G (p.Pro87Ala)	not specified [RCV004654835]	uncertain significance	2	241814949	241814949	Human		name
597639926	CV3565701	single nucleotide variant	NM_001167600.3(NEU4):c.148C>T (p.His50Tyr)	not specified [RCV004832015]	uncertain significance	2	241814632	241814632	Human		name
597639953	CV3565706	single nucleotide variant	NM_001167600.3(NEU4):c.175G>A (p.Gly59Ser)	not specified [RCV004832019]	uncertain significance	2	241814659	241814659	Human		name
597639978	CV3565710	single nucleotide variant	NM_001167600.3(NEU4):c.184G>T (p.Ala62Ser)	not specified [RCV004832023]	uncertain significance	2	241814668	241814668	Human		name
598232293	CV4000525	single nucleotide variant	NM_001167600.3(NEU4):c.248G>T (p.Arg83Leu)	not specified [RCV005381517]	uncertain significance	2	241814938	241814938	Human		name
598232309	CV4000528	single nucleotide variant	NM_001167600.3(NEU4):c.233C>T (p.Ala78Val)	not specified [RCV005381520]	uncertain significance	2	241814923	241814923	Human		name
156371672	CV2200882	single nucleotide variant	NM_001167600.3(NEU4):c.418C>T (p.Arg140Trp)	not specified [RCV004081504]	uncertain significance	2	241815108	241815108	Human		name
156069973	CV2203900	single nucleotide variant	NM_001167600.3(NEU4):c.419G>A (p.Arg140Gln)	not specified [RCV004069951]	uncertain significance	2	241815109	241815109	Human		name
156380221	CV2208010	single nucleotide variant	NM_001167600.3(NEU4):c.397G>A (p.Gly133Ser)	not specified [RCV004086712]	uncertain significance	2	241815087	241815087	Human		name
156060589	CV2239464	single nucleotide variant	NM_001167600.3(NEU4):c.368G>A (p.Arg123His)	not specified [RCV004114180]	uncertain significance	2	241815058	241815058	Human		name
156278943	CV2252124	single nucleotide variant	NM_001167600.3(NEU4):c.526G>A (p.Ala176Thr)	not specified [RCV004122148]	uncertain significance	2	241816119	241816119	Human		name
156175406	CV2278204	single nucleotide variant	NM_001167600.3(NEU4):c.514C>G (p.Leu172Val)	not specified [RCV004141394]	uncertain significance	2	241816107	241816107	Human		name
156171274	CV2337496	single nucleotide variant	NM_001167600.3(NEU4):c.575G>A (p.Arg192Gln)	not specified [RCV004187929]	uncertain significance	2	241816168	241816168	Human		name
155983986	CV2348177	single nucleotide variant	NM_001167600.3(NEU4):c.875G>A (p.Arg292Gln)	not specified [RCV004190820]	uncertain significance	2	241816468	241816468	Human		name
329378698	CV2447086	single nucleotide variant	NM_001167600.3(NEU4):c.628C>T (p.Arg210Cys)	not specified [RCV004259960]	uncertain significance	2	241816221	241816221	Human		name
401721924	CV2680743	single nucleotide variant	NM_001167600.3(NEU4):c.580A>G (p.Ser194Gly)	not specified [RCV004291352]	uncertain significance	2	241816173	241816173	Human		name
401751178	CV2712438	single nucleotide variant	NM_001167600.3(NEU4):c.376T>C (p.Cys126Arg)	not specified [RCV004313901]	uncertain significance	2	241815066	241815066	Human		name
401752703	CV2723325	single nucleotide variant	NM_001167600.3(NEU4):c.656G>A (p.Arg219His)	not specified [RCV004329544]	uncertain significance	2	241816249	241816249	Human		name
401780348	CV2726007	single nucleotide variant	NM_001167600.3(NEU4):c.350C>T (p.Thr117Met)	not specified [RCV004324369]	uncertain significance	2	241815040	241815040	Human		name
401745932	CV2734295	single nucleotide variant	NM_001167600.3(NEU4):c.511C>T (p.Arg171Cys)	not specified [RCV004332524]	uncertain significance	2	241816104	241816104	Human		name
401855869	CV2757574	single nucleotide variant	NM_001167600.3(NEU4):c.962C>T (p.Ala321Val)	not specified [RCV004340944]	uncertain significance	2	241816555	241816555	Human		name
401891089	CV2778637	single nucleotide variant	NM_001167600.3(NEU4):c.794G>A (p.Arg265His)	not specified [RCV004344282]	uncertain significance	2	241816387	241816387	Human		name
401930436	CV2827014	single nucleotide variant	NM_001167600.3(NEU4):c.430G>A (p.Glu144Lys)	not provided [RCV003440299]	likely benign	2	241815120	241815120	Human		name
405711557	CV3350351	single nucleotide variant	NM_001167600.3(NEU4):c.991G>A (p.Gly331Ser)	not specified [RCV004493925]	uncertain significance	2	241816584	241816584	Human		name
405712336	CV3350455	single nucleotide variant	NM_001167600.3(NEU4):c.415G>T (p.Ala139Ser)	not specified [RCV004494029]	uncertain significance	2	241815105	241815105	Human		name
405712385	CV3350462	single nucleotide variant	NM_001167600.3(NEU4):c.472G>A (p.Ala158Thr)	not specified [RCV004494036]	uncertain significance	2	241816065	241816065	Human		name
405712487	CV3350478	single nucleotide variant	NM_001167600.3(NEU4):c.551G>A (p.Arg184Gln)	not specified [RCV004494052]	uncertain significance	2	241816144	241816144	Human		name
405712553	CV3350487	single nucleotide variant	NM_001167600.3(NEU4):c.637G>A (p.Gly213Ser)	not specified [RCV004494061]	uncertain significance	2	241816230	241816230	Human		name
405712577	CV3350491	single nucleotide variant	NM_001167600.3(NEU4):c.700G>A (p.Gly234Ser)	not specified [RCV004494065]	uncertain significance	2	241816293	241816293	Human		name
405712584	CV3350492	single nucleotide variant	NM_001167600.3(NEU4):c.707T>C (p.Phe236Ser)	not specified [RCV004494066]	uncertain significance	2	241816300	241816300	Human		name
405712617	CV3350497	single nucleotide variant	NM_001167600.3(NEU4):c.773C>G (p.Thr258Ser)	not specified [RCV004494071]	uncertain significance	2	241816366	241816366	Human		name
405712679	CV3350506	single nucleotide variant	NM_001167600.3(NEU4):c.859G>A (p.Ala287Thr)	not specified [RCV004494080]	uncertain significance	2	241816452	241816452	Human		name
407526494	CV3451048	single nucleotide variant	NM_001167600.3(NEU4):c.619C>T (p.Arg207Cys)	not specified [RCV004654831]	uncertain significance	2	241816212	241816212	Human		name
407526497	CV3451049	single nucleotide variant	NM_001167600.3(NEU4):c.893T>C (p.Val298Ala)	not specified [RCV004654832]	uncertain significance	2	241816486	241816486	Human		name
407526503	CV3451051	single nucleotide variant	NM_001167600.3(NEU4):c.382G>T (p.Ala128Ser)	not specified [RCV004654834]	uncertain significance	2	241815072	241815072	Human		name
407489763	CV3451053	single nucleotide variant	NM_001167600.3(NEU4):c.811G>A (p.Glu271Lys)	not specified [RCV004641532]	uncertain significance	2	241816404	241816404	Human		name
597639906	CV3565698	single nucleotide variant	NM_001167600.3(NEU4):c.388C>T (p.Arg130Cys)	not specified [RCV004832012]	uncertain significance	2	241815078	241815078	Human		name
597639921	CV3565700	single nucleotide variant	NM_001167600.3(NEU4):c.803C>T (p.Ser268Phe)	not specified [RCV004832014]	uncertain significance	2	241816396	241816396	Human		name
597639932	CV3565703	single nucleotide variant	NM_001167600.3(NEU4):c.367C>T (p.Arg123Cys)	not specified [RCV004832016]	uncertain significance	2	241815057	241815057	Human		name
597639939	CV3565704	single nucleotide variant	NM_001167600.3(NEU4):c.526G>C (p.Ala176Pro)	not specified [RCV004832017]	uncertain significance	2	241816119	241816119	Human		name
597639966	CV3565708	single nucleotide variant	NM_001167600.3(NEU4):c.629G>A (p.Arg210His)	not specified [RCV004832021]	likely benign	2	241816222	241816222	Human		name
598232304	CV4000527	single nucleotide variant	NM_001167600.3(NEU4):c.785C>T (p.Pro262Leu)	not specified [RCV005381519]	uncertain significance	2	241816378	241816378	Human		name
598254741	CV4000529	single nucleotide variant	NM_001167600.3(NEU4):c.415G>A (p.Ala139Thr)	not specified [RCV005385543]	uncertain significance	2	241815105	241815105	Human		name
598232314	CV4000530	single nucleotide variant	NM_001167600.3(NEU4):c.757A>G (p.Ser253Gly)	not specified [RCV005381521]	uncertain significance	2	241816350	241816350	Human		name
598232319	CV4000532	single nucleotide variant	NM_001167600.3(NEU4):c.419G>C (p.Arg140Pro)	not specified [RCV005381522]	uncertain significance	2	241815109	241815109	Human		name
155960904	CV2204388	single nucleotide variant	NM_001167600.3(NEU4):c.1261G>A (p.Asp421Asn)	not specified [RCV004079204]	uncertain significance	2	241816854	241816854	Human		name
156176327	CV2258087	single nucleotide variant	NM_001167600.3(NEU4):c.1433G>A (p.Arg478Gln)	not specified [RCV004121482]	uncertain significance	2	241817026	241817026	Human		name
156242918	CV2262196	single nucleotide variant	NM_001167600.3(NEU4):c.1046C>T (p.Pro349Leu)	not specified [RCV004126627]	uncertain significance	2	241816639	241816639	Human		name
156286637	CV2327256	single nucleotide variant	NM_001167600.3(NEU4):c.1157G>A (p.Arg386His)	not specified [RCV004174706]	uncertain significance	2	241816750	241816750	Human		name
156286543	CV2334942	single nucleotide variant	NM_001167600.3(NEU4):c.1318G>C (p.Glu440Gln)	not specified [RCV004182043]	uncertain significance	2	241816911	241816911	Human		name
155922271	CV2350801	single nucleotide variant	NM_001167600.3(NEU4):c.1199C>T (p.Pro400Leu)	not specified [RCV004207134]	uncertain significance	2	241816792	241816792	Human		name
156198444	CV2357864	single nucleotide variant	NM_001167600.3(NEU4):c.1003A>G (p.Ser335Gly)	not specified [RCV004205145]	uncertain significance	2	241816596	241816596	Human		name
155918241	CV2362544	single nucleotide variant	NM_001167600.3(NEU4):c.1279C>T (p.Pro427Ser)	not specified [RCV004215208]	uncertain significance	2	241816872	241816872	Human		name
156343816	CV2364170	single nucleotide variant	NM_001167600.3(NEU4):c.1372C>T (p.Arg458Cys)	not specified [RCV004223413]	uncertain significance	2	241816965	241816965	Human		name
155930721	CV2399710	single nucleotide variant	NM_001167600.3(NEU4):c.1276G>A (p.Gly426Arg)	not specified [RCV004245528]	uncertain significance	2	241816869	241816869	Human		name
156007376	CV2401305	single nucleotide variant	NM_001167600.3(NEU4):c.1357T>C (p.Cys453Arg)	not specified [RCV004245846]	uncertain significance	2	241816950	241816950	Human		name
401779949	CV2676747	single nucleotide variant	NM_001167600.3(NEU4):c.1445G>T (p.Trp482Leu)	not specified [RCV004290921]	uncertain significance	2	241817038	241817038	Human		name
401737487	CV2679893	single nucleotide variant	NM_001167600.3(NEU4):c.1372C>A (p.Arg458Ser)	not specified [RCV004284181]	uncertain significance	2	241816965	241816965	Human		name
401883760	CV2754975	single nucleotide variant	NM_001167600.3(NEU4):c.1409C>T (p.Pro470Leu)	not specified [RCV004341440]	uncertain significance	2	241817002	241817002	Human		name
401882831	CV2775117	single nucleotide variant	NM_001167600.3(NEU4):c.1208C>T (p.Pro403Leu)	not specified [RCV004346478]	uncertain significance	2	241816801	241816801	Human		name
405711716	CV3350372	single nucleotide variant	NM_001167600.3(NEU4):c.1146C>G (p.His382Gln)	not specified [RCV004493946]	uncertain significance	2	241816739	241816739	Human		name
405711811	CV3350385	single nucleotide variant	NM_001167600.3(NEU4):c.1236C>G (p.Ile412Met)	not specified [RCV004493959]	uncertain significance	2	241816829	241816829	Human		name
405711923	CV3350400	single nucleotide variant	NM_001167600.3(NEU4):c.1280C>T (p.Pro427Leu)	not specified [RCV004493974]	uncertain significance	2	241816873	241816873	Human		name
405711965	CV3350405	single nucleotide variant	NM_001167600.3(NEU4):c.1283C>T (p.Ala428Val)	not specified [RCV004493979]	uncertain significance	2	241816876	241816876	Human		name
405711980	CV3350407	single nucleotide variant	NM_001167600.3(NEU4):c.1291G>T (p.Gly431Trp)	not specified [RCV004493981]	uncertain significance	2	241816884	241816884	Human		name
597639914	CV3565699	single nucleotide variant	NM_001167600.3(NEU4):c.1184G>A (p.Arg395His)	not specified [RCV004832013]	uncertain significance	2	241816777	241816777	Human		name
597639946	CV3565705	single nucleotide variant	NM_001167600.3(NEU4):c.1292G>A (p.Gly431Glu)	not specified [RCV004832018]	uncertain significance	2	241816885	241816885	Human		name
597639972	CV3565709	single nucleotide variant	NM_001167600.3(NEU4):c.1403C>T (p.Pro468Leu)	not specified [RCV004832022]	uncertain significance	2	241816996	241816996	Human		name
598232298	CV4000526	single nucleotide variant	NM_001167600.3(NEU4):c.1432C>T (p.Arg478Trp)	not specified [RCV005381518]	uncertain significance	2	241817025	241817025	Human		name

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