Oas3 Variant Search Result - Rat Genome Database

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127 records found for search term Oas3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597666538	CV3566956	single nucleotide variant	NM_006187.4(OAS3):c.8T>C (p.Leu3Ser)	not specified [RCV004835738]	uncertain significance	12	112938538	112938538	Human		name
156375169	CV2213517	single nucleotide variant	NM_006187.4(OAS3):c.92G>A (p.Arg31His)	not specified [RCV004087481]	uncertain significance	12	112938622	112938622	Human		name
156348034	CV2383030	single nucleotide variant	NM_006187.4(OAS3):c.79G>A (p.Glu27Lys)	not specified [RCV004217613]	uncertain significance	12	112938609	112938609	Human		name
598221809	CV3893786	single nucleotide variant	NM_006187.4(OAS3):c.312G>A (p.Ser104=)	not provided [RCV005257029]	benign	12	112941704	112941704	Human		name
156368952	CV2193829	single nucleotide variant	NM_006187.4(OAS3):c.128G>C (p.Arg43Pro)	not specified [RCV004074578]	uncertain significance	12	112938658	112938658	Human		name
156007663	CV2288329	single nucleotide variant	NM_006187.4(OAS3):c.121A>T (p.Arg41Trp)	not specified [RCV004150100]	uncertain significance	12	112938651	112938651	Human		name
329359874	CV2462350	single nucleotide variant	NM_006187.4(OAS3):c.281G>A (p.Arg94His)	not specified [RCV004266333]	uncertain significance	12	112941673	112941673	Human		name
329398028	CV2466555	single nucleotide variant	NM_006187.4(OAS3):c.178G>A (p.Gly60Arg)	not specified [RCV004274091]	uncertain significance	12	112941570	112941570	Human		name
401733280	CV2685479	single nucleotide variant	NM_006187.4(OAS3):c.157C>T (p.Arg53Trp)	not specified [RCV004294502]	uncertain significance	12	112938687	112938687	Human		name
405731616	CV3362925	single nucleotide variant	NM_006187.4(OAS3):c.124G>A (p.Glu42Lys)	not specified [RCV004496463]	uncertain significance	12	112938654	112938654	Human		name
405731632	CV3362927	single nucleotide variant	NM_006187.4(OAS3):c.158G>A (p.Arg53Gln)	not specified [RCV004496465]	uncertain significance	12	112938688	112938688	Human		name
597666501	CV3566950	single nucleotide variant	NM_006187.4(OAS3):c.277C>T (p.Arg93Cys)	not specified [RCV004835733]	uncertain significance	12	112941669	112941669	Human		name
15156261	CV713343	single nucleotide variant	NM_006187.4(OAS3):c.145G>A (p.Ala49Thr)	not provided [RCV000969080]	benign	12	112938675	112938675	Human		name
8634508	CV89728	single nucleotide variant	NM_006187.3(OAS3):c.1191C>T (p.Ile397=)	Malignant melanoma [RCV000069825]	not provided	12	112949022	112949022	Human		name
156182464	CV2201893	single nucleotide variant	NM_006187.4(OAS3):c.583C>T (p.Arg195Cys)	not specified [RCV004082315]	uncertain significance	12	112944598	112944598	Human		name
156048771	CV2220219	single nucleotide variant	NM_006187.4(OAS3):c.844C>A (p.Gln282Lys)	not specified [RCV004095670]	uncertain significance	12	112946950	112946950	Human		name
156212444	CV2259952	single nucleotide variant	NM_006187.4(OAS3):c.845A>G (p.Gln282Arg)	not specified [RCV004118975]	uncertain significance	12	112946951	112946951	Human		name
156190321	CV2325470	single nucleotide variant	NM_006187.4(OAS3):c.364G>A (p.Glu122Lys)	not specified [RCV004179923]	uncertain significance	12	112941756	112941756	Human		name
156402044	CV2367883	single nucleotide variant	NM_006187.4(OAS3):c.535G>A (p.Glu179Lys)	not specified [RCV004222985]	uncertain significance	12	112944550	112944550	Human		name
156338009	CV2370542	single nucleotide variant	NM_006187.4(OAS3):c.689A>G (p.Glu230Gly)	not specified [RCV004215876]	uncertain significance	12	112946795	112946795	Human		name
329364019	CV2469637	single nucleotide variant	NM_006187.4(OAS3):c.506C>T (p.Thr169Ile)	not specified [RCV004283061]	uncertain significance	12	112944521	112944521	Human		name
401747512	CV2691610	single nucleotide variant	NM_006187.4(OAS3):c.718G>A (p.Gly240Ser)	not specified [RCV004305433]	uncertain significance	12	112946824	112946824	Human		name
401721866	CV2710205	single nucleotide variant	NM_006187.4(OAS3):c.629A>G (p.Tyr210Cys)	not specified [RCV004317106]	uncertain significance	12	112944644	112944644	Human		name
405731779	CV3362946	single nucleotide variant	NM_006187.4(OAS3):c.393C>G (p.Phe131Leu)	not specified [RCV004496484]	uncertain significance	12	112941785	112941785	Human		name
405731790	CV3362948	single nucleotide variant	NM_006187.4(OAS3):c.826G>A (p.Glu276Lys)	not specified [RCV004496486]	uncertain significance	12	112946932	112946932	Human		name
405731799	CV3362949	single nucleotide variant	NM_006187.4(OAS3):c.887T>C (p.Leu296Pro)	not specified [RCV004496487]	uncertain significance	12	112947957	112947957	Human		name
405731808	CV3362950	single nucleotide variant	NM_006187.4(OAS3):c.907T>G (p.Trp303Gly)	not specified [RCV004496488]	uncertain significance	12	112947977	112947977	Human		name
405731816	CV3362951	single nucleotide variant	NM_006187.4(OAS3):c.961G>A (p.Ala321Thr)	not specified [RCV004496489]	uncertain significance	12	112948031	112948031	Human		name
407478454	CV3459214	single nucleotide variant	NM_006187.4(OAS3):c.503C>G (p.Ser168Cys)	not specified [RCV004639003]	uncertain significance	12	112944518	112944518	Human		name
407478460	CV3459215	single nucleotide variant	NM_006187.4(OAS3):c.532G>C (p.Gly178Arg)	not specified [RCV004639004]	uncertain significance	12	112944547	112944547	Human		name
407522545	CV3459218	single nucleotide variant	NM_006187.4(OAS3):c.395G>A (p.Arg132His)	not specified [RCV004652881]	uncertain significance	12	112941787	112941787	Human		name
407522552	CV3459220	single nucleotide variant	NM_006187.4(OAS3):c.452A>G (p.Asn151Ser)	not specified [RCV004652883]	uncertain significance	12	112941844	112941844	Human		name
597666487	CV3566948	single nucleotide variant	NM_006187.4(OAS3):c.347T>C (p.Leu116Pro)	not specified [RCV004835731]	uncertain significance	12	112941739	112941739	Human		name
597666516	CV3566952	single nucleotide variant	NM_006187.4(OAS3):c.665C>T (p.Thr222Met)	not specified [RCV004835735]	uncertain significance	12	112946771	112946771	Human		name
597666545	CV3566957	single nucleotide variant	NM_006187.4(OAS3):c.508C>G (p.Leu170Val)	not specified [RCV004835739]	uncertain significance	12	112944523	112944523	Human		name
597659579	CV3566963	single nucleotide variant	NM_006187.4(OAS3):c.992G>A (p.Arg331Lys)	not specified [RCV004834786]	uncertain significance	12	112948062	112948062	Human		name
597666571	CV3566964	single nucleotide variant	NM_006187.4(OAS3):c.475G>A (p.Gly159Ser)	not specified [RCV004835743]	uncertain significance	12	112944490	112944490	Human		name
598194410	CV4001163	single nucleotide variant	NM_006187.4(OAS3):c.311C>T (p.Ser104Leu)	not specified [RCV005374712]	likely benign	12	112941703	112941703	Human		name
598194419	CV4001164	single nucleotide variant	NM_006187.4(OAS3):c.719G>T (p.Gly240Val)	not specified [RCV005374713]	uncertain significance	12	112946825	112946825	Human		name
598194425	CV4001165	single nucleotide variant	NM_006187.4(OAS3):c.374T>A (p.Val125Glu)	not specified [RCV005374714]	uncertain significance	12	112941766	112941766	Human		name
598194440	CV4001168	single nucleotide variant	NM_006187.4(OAS3):c.305G>A (p.Arg102Gln)	not specified [RCV005374716]	uncertain significance	12	112941697	112941697	Human		name
598194453	CV4001170	single nucleotide variant	NM_006187.4(OAS3):c.470G>T (p.Gly157Val)	not specified [RCV005374718]	uncertain significance	12	112944485	112944485	Human		name
598194483	CV4001175	single nucleotide variant	NM_006187.4(OAS3):c.721T>C (p.Cys241Arg)	not specified [RCV005374722]	uncertain significance	12	112946827	112946827	Human		name
150478044	CV1218721	single nucleotide variant	NM_006187.4(OAS3):c.1143C>G (p.Ser381Arg)	not provided [RCV001616348]	benign	12	112948974	112948974	Human		name
156164822	CV2195908	single nucleotide variant	NM_006187.4(OAS3):c.2065G>A (p.Gly689Ser)	not specified [RCV004072168]	uncertain significance	12	112962883	112962883	Human		name
156042605	CV2215783	single nucleotide variant	NM_006187.4(OAS3):c.2194A>G (p.Arg732Gly)	not specified [RCV004095378]	likely benign	12	112963422	112963422	Human		name
156286341	CV2232945	single nucleotide variant	NM_006187.4(OAS3):c.2440C>T (p.Arg814Cys)	not specified [RCV004103324]	uncertain significance	12	112965780	112965780	Human		name
156071977	CV2251457	single nucleotide variant	NM_006187.4(OAS3):c.1246C>A (p.Leu416Met)	not specified [RCV004117436]	uncertain significance	12	112949077	112949077	Human		name
156304080	CV2255504	single nucleotide variant	NM_006187.4(OAS3):c.1760G>A (p.Arg587Gln)	not specified [RCV004119938]	uncertain significance	12	112961173	112961173	Human		name
155949418	CV2267641	single nucleotide variant	NM_006187.4(OAS3):c.1382C>T (p.Ser461Leu)	not specified [RCV004134192]	uncertain significance	12	112950700	112950700	Human		name
156360955	CV2269145	single nucleotide variant	NM_006187.4(OAS3):c.1166C>T (p.Pro389Leu)	not specified [RCV004130317]	uncertain significance	12	112948997	112948997	Human		name
156051719	CV2269378	single nucleotide variant	NM_006187.4(OAS3):c.2635A>G (p.Thr879Ala)	not specified [RCV004124509]	uncertain significance	12	112965975	112965975	Human		name
156037996	CV2313599	single nucleotide variant	NM_006187.4(OAS3):c.2774C>T (p.Thr925Ile)	not specified [RCV004157536]	uncertain significance	12	112967502	112967502	Human		name
156063291	CV2316757	single nucleotide variant	NM_006187.4(OAS3):c.2884G>A (p.Gly962Arg)	not specified [RCV004171978]	uncertain significance	12	112967954	112967954	Human		name
156276203	CV2318475	single nucleotide variant	NM_006187.4(OAS3):c.1967G>A (p.Arg656Gln)	not specified [RCV004173121]	uncertain significance	12	112962785	112962785	Human		name
156326081	CV2335409	single nucleotide variant	NM_006187.4(OAS3):c.2641C>G (p.Leu881Val)	not specified [RCV004186963]	uncertain significance	12	112965981	112965981	Human		name
156216759	CV2348054	single nucleotide variant	NM_006187.4(OAS3):c.2839C>T (p.Arg947Trp)	not specified [RCV004197736]	uncertain significance	12	112967567	112967567	Human		name
156068746	CV2355697	single nucleotide variant	NM_006187.4(OAS3):c.2483A>T (p.Gln828Leu)	not specified [RCV004199059]	uncertain significance	12	112965823	112965823	Human		name
156255676	CV2359442	single nucleotide variant	NM_006187.4(OAS3):c.1253G>A (p.Arg418His)	not specified [RCV004214764]	uncertain significance	12	112949084	112949084	Human		name
156106611	CV2370950	single nucleotide variant	NM_006187.4(OAS3):c.2608G>A (p.Val870Met)	not specified [RCV004218677]	uncertain significance	12	112965948	112965948	Human		name
155934169	CV2372409	single nucleotide variant	NM_006187.4(OAS3):c.1118A>G (p.Asn373Ser)	not specified [RCV004217173]	uncertain significance	12	112948949	112948949	Human		name
329366121	CV2438127	single nucleotide variant	NM_006187.4(OAS3):c.2165C>G (p.Ala722Gly)	not specified [RCV004256907]	uncertain significance	12	112963393	112963393	Human		name
329363049	CV2449702	single nucleotide variant	NM_006187.4(OAS3):c.2375C>A (p.Ser792Tyr)	not specified [RCV004268603]	uncertain significance	12	112964380	112964380	Human		name
401729153	CV2673170	single nucleotide variant	NM_006187.4(OAS3):c.2682C>A (p.Asp894Glu)	not specified [RCV004284149]	uncertain significance	12	112966022	112966022	Human		name
401766480	CV2679708	single nucleotide variant	NM_006187.4(OAS3):c.1642G>T (p.Ala548Ser)	not specified [RCV004282178]	uncertain significance	12	112950960	112950960	Human		name
401766482	CV2679709	single nucleotide variant	NM_006187.4(OAS3):c.1643C>T (p.Ala548Val)	not specified [RCV004282179]	uncertain significance	12	112950961	112950961	Human		name
401727210	CV2684515	single nucleotide variant	NM_006187.4(OAS3):c.1129C>A (p.Pro377Thr)	not specified [RCV004291585]	uncertain significance	12	112948960	112948960	Human		name
401774466	CV2691746	single nucleotide variant	NM_006187.4(OAS3):c.2260G>A (p.Asp754Asn)	not specified [RCV004299202]	uncertain significance	12	112964265	112964265	Human		name
401778289	CV2718639	single nucleotide variant	NM_006187.4(OAS3):c.1085A>G (p.Asn362Ser)	not specified [RCV004320218]	uncertain significance	12	112948916	112948916	Human		name
401862649	CV2762300	single nucleotide variant	NM_006187.4(OAS3):c.1451C>T (p.Thr484Met)	not specified [RCV004335416]	uncertain significance	12	112950769	112950769	Human		name
401864082	CV2781476	single nucleotide variant	NM_006187.4(OAS3):c.1375G>T (p.Gly459Trp)	not specified [RCV004354712]	uncertain significance	12	112950693	112950693	Human		name
405731602	CV3362924	single nucleotide variant	NM_006187.4(OAS3):c.1054G>A (p.Gly352Ser)	not specified [RCV004496462]	uncertain significance	12	112948885	112948885	Human		name
405731624	CV3362926	single nucleotide variant	NM_006187.4(OAS3):c.1326G>C (p.Leu442Phe)	not specified [RCV004496464]	uncertain significance	12	112949157	112949157	Human		name
405731640	CV3362928	single nucleotide variant	NM_006187.4(OAS3):c.1773G>T (p.Met591Ile)	not specified [RCV004496466]	uncertain significance	12	112961186	112961186	Human		name
405731649	CV3362929	single nucleotide variant	NM_006187.4(OAS3):c.1781G>A (p.Arg594His)	not specified [RCV004496467]	uncertain significance	12	112961194	112961194	Human		name
405731654	CV3362930	single nucleotide variant	NM_006187.4(OAS3):c.1829G>A (p.Arg610His)	not specified [RCV004496468]	uncertain significance	12	112961242	112961242	Human		name
405731669	CV3362932	single nucleotide variant	NM_006187.4(OAS3):c.1838C>T (p.Ala613Val)	not specified [RCV004496470]	uncertain significance	12	112962656	112962656	Human		name
405731676	CV3362933	single nucleotide variant	NM_006187.4(OAS3):c.1861C>A (p.Pro621Thr)	not specified [RCV004496471]	uncertain significance	12	112962679	112962679	Human		name
405731684	CV3362934	single nucleotide variant	NM_006187.4(OAS3):c.1907C>G (p.Thr636Ser)	not specified [RCV004496472]	uncertain significance	12	112962725	112962725	Human		name
405731691	CV3362935	single nucleotide variant	NM_006187.4(OAS3):c.1966C>T (p.Arg656Trp)	not specified [RCV004496473]	uncertain significance	12	112962784	112962784	Human		name
405731700	CV3362936	single nucleotide variant	NM_006187.4(OAS3):c.1976T>C (p.Leu659Pro)	not specified [RCV004496474]	uncertain significance	12	112962794	112962794	Human		name
405731706	CV3362937	single nucleotide variant	NM_006187.4(OAS3):c.2045C>G (p.Ala682Gly)	not specified [RCV004496475]	uncertain significance	12	112962863	112962863	Human		name
405731720	CV3362939	single nucleotide variant	NM_006187.4(OAS3):c.2636C>T (p.Thr879Met)	not specified [RCV004496477]	uncertain significance	12	112965976	112965976	Human		name
405731730	CV3362940	single nucleotide variant	NM_006187.4(OAS3):c.2786A>G (p.Glu929Gly)	not specified [RCV004496478]	uncertain significance	12	112967514	112967514	Human		name
405731736	CV3362941	single nucleotide variant	NM_006187.4(OAS3):c.2929G>A (p.Val977Met)	not specified [RCV004496479]	uncertain significance	12	112967999	112967999	Human		name
407522540	CV3459213	single nucleotide variant	NM_006187.4(OAS3):c.2987G>A (p.Arg996His)	not specified [RCV004652879]	uncertain significance	12	112968057	112968057	Human		name
407478464	CV3459216	single nucleotide variant	NM_006187.4(OAS3):c.1627G>A (p.Val543Ile)	not specified [RCV004639005]	uncertain significance	12	112950945	112950945	Human		name
407522543	CV3459217	single nucleotide variant	NM_006187.4(OAS3):c.1082C>A (p.Pro361His)	not specified [RCV004652880]	uncertain significance	12	112948913	112948913	Human		name
407522549	CV3459219	single nucleotide variant	NM_006187.4(OAS3):c.1405A>G (p.Arg469Gly)	not specified [RCV004652882]	uncertain significance	12	112950723	112950723	Human		name
407522555	CV3459221	single nucleotide variant	NM_006187.4(OAS3):c.1648G>C (p.Asp550His)	not specified [RCV004652884]	uncertain significance	12	112950966	112950966	Human		name
596946954	CV3547012	single nucleotide variant	NM_006187.4(OAS3):c.2795G>A (p.Arg932Gln)	not provided [RCV004810818]	likely benign	12	112967523	112967523	Human		name
597666478	CV3566947	single nucleotide variant	NM_006187.4(OAS3):c.1477C>T (p.Arg493Cys)	not specified [RCV004835730]	uncertain significance	12	112950795	112950795	Human		name
597666493	CV3566949	single nucleotide variant	NM_006187.4(OAS3):c.1970C>T (p.Thr657Met)	not specified [RCV004835732]	uncertain significance	12	112962788	112962788	Human		name
597666508	CV3566951	single nucleotide variant	NM_006187.4(OAS3):c.1328G>A (p.Arg443His)	not specified [RCV004835734]	uncertain significance	12	112949159	112949159	Human		name
597666523	CV3566953	single nucleotide variant	NM_006187.4(OAS3):c.2987G>T (p.Arg996Leu)	not specified [RCV004835736]	uncertain significance	12	112968057	112968057	Human		name
597659555	CV3566954	single nucleotide variant	NM_006187.4(OAS3):c.2990C>T (p.Thr997Met)	not specified [RCV004834783]	uncertain significance	12	112968060	112968060	Human		name
597666528	CV3566955	single nucleotide variant	NM_006187.4(OAS3):c.1505C>T (p.Ala502Val)	not specified [RCV004835737]	uncertain significance	12	112950823	112950823	Human		name
597666549	CV3566958	single nucleotide variant	NM_006187.4(OAS3):c.1790A>G (p.Lys597Arg)	not specified [RCV004835740]	uncertain significance	12	112961203	112961203	Human		name
597659564	CV3566959	single nucleotide variant	NM_006187.4(OAS3):c.2509G>A (p.Ala837Thr)	not specified [RCV004834784]	uncertain significance	12	112965849	112965849	Human		name
597666556	CV3566960	single nucleotide variant	NM_006187.4(OAS3):c.1159C>T (p.Pro387Ser)	not specified [RCV004835741]	uncertain significance	12	112948990	112948990	Human		name
597666563	CV3566961	single nucleotide variant	NM_006187.4(OAS3):c.2910C>A (p.His970Gln)	not specified [RCV004835742]	uncertain significance	12	112967980	112967980	Human		name
597659571	CV3566962	single nucleotide variant	NM_006187.4(OAS3):c.2234C>T (p.Ala745Val)	not specified [RCV004834785]	uncertain significance	12	112964239	112964239	Human		name
597666578	CV3566965	single nucleotide variant	NM_006187.4(OAS3):c.1778T>C (p.Ile593Thr)	not specified [RCV004835744]	likely benign	12	112961191	112961191	Human		name
597666587	CV3566966	single nucleotide variant	NM_006187.4(OAS3):c.2840G>A (p.Arg947Gln)	not specified [RCV004835745]	uncertain significance	12	112967568	112967568	Human		name
597666595	CV3566967	single nucleotide variant	NM_006187.4(OAS3):c.1521G>C (p.Trp507Cys)	not specified [RCV004835746]	uncertain significance	12	112950839	112950839	Human		name
597666602	CV3566968	single nucleotide variant	NM_006187.4(OAS3):c.1099G>A (p.Glu367Lys)	not specified [RCV004835747]	uncertain significance	12	112948930	112948930	Human		name
597666612	CV3566969	single nucleotide variant	NM_006187.4(OAS3):c.2683G>A (p.Ala895Thr)	not specified [RCV004835748]	uncertain significance	12	112966023	112966023	Human		name
598194432	CV4001166	single nucleotide variant	NM_006187.4(OAS3):c.1261C>G (p.Gln421Glu)	not specified [RCV005374715]	uncertain significance	12	112949092	112949092	Human		name
598159502	CV4001167	single nucleotide variant	NM_006187.4(OAS3):c.1009G>A (p.Val337Met)	not specified [RCV005390178]	uncertain significance	12	112948079	112948079	Human		name
598194446	CV4001169	single nucleotide variant	NM_006187.4(OAS3):c.1243G>A (p.Glu415Lys)	not specified [RCV005374717]	uncertain significance	12	112949074	112949074	Human		name
598159506	CV4001171	single nucleotide variant	NM_006187.4(OAS3):c.2572G>A (p.Val858Ile)	not specified [RCV005390179]	uncertain significance	12	112965912	112965912	Human		name
598194467	CV4001173	single nucleotide variant	NM_006187.4(OAS3):c.1148C>G (p.Pro383Arg)	not specified [RCV005374720]	uncertain significance	12	112948979	112948979	Human		name
598159510	CV4001176	single nucleotide variant	NM_006187.4(OAS3):c.1255T>C (p.Phe419Leu)	not specified [RCV005390180]	uncertain significance	12	112949086	112949086	Human		name
617152333	CV4020702	single nucleotide variant	NM_006187.4(OAS3):c.2530C>T (p.Arg844Ter)	not provided [RCV005427959]	benign	12	112965870	112965870	Human		name
15174139	CV679113	single nucleotide variant	NM_006187.4(OAS3):c.1390C>T (p.Arg464Trp)	Aganglionic megacolon [RCV000984693]	uncertain significance	12	112950708	112950708	Human	2	name
15187109	CV702134	single nucleotide variant	NM_006187.4(OAS3):c.1475G>A (p.Arg492His)	not provided [RCV000953489]	benign	12	112950793	112950793	Human		name
15104675	CV702135	single nucleotide variant	NM_006187.4(OAS3):c.2179G>T (p.Ala727Ser)	not provided [RCV000959732]	benign	12	112963407	112963407	Human		name
156270453	CV2195165	single nucleotide variant	NM_006187.4(OAS3):c.3256G>C (p.Ala1086Pro)	not specified [RCV004080113]	uncertain significance	12	112969965	112969965	Human		name
156278314	CV2252073	single nucleotide variant	NM_006187.4(OAS3):c.3226A>G (p.Ile1076Val)	not specified [RCV004122102]	uncertain significance	12	112969729	112969729	Human		name
156075818	CV2331762	single nucleotide variant	NM_006187.4(OAS3):c.3131C>T (p.Pro1044Leu)	not specified [RCV004184386]	uncertain significance	12	112969634	112969634	Human		name
155993229	CV2381743	single nucleotide variant	NM_006187.4(OAS3):c.3091C>A (p.Leu1031Ile)	not specified [RCV004232197]	uncertain significance	12	112968161	112968161	Human		name
329377398	CV2462599	single nucleotide variant	NM_006187.4(OAS3):c.3241T>C (p.Trp1081Arg)	not specified [RCV004278545]	uncertain significance	12	112969744	112969744	Human		name
329380843	CV2464375	single nucleotide variant	NM_006187.4(OAS3):c.3052G>A (p.Ala1018Thr)	not specified [RCV004276318]	likely benign	12	112968122	112968122	Human		name
405731745	CV3362942	single nucleotide variant	NM_006187.4(OAS3):c.3016C>T (p.Arg1006Cys)	not specified [RCV004496480]	uncertain significance	12	112968086	112968086	Human		name
405731755	CV3362943	single nucleotide variant	NM_006187.4(OAS3):c.3017G>A (p.Arg1006His)	not specified [RCV004496481]	uncertain significance	12	112968087	112968087	Human		name
405731770	CV3362945	single nucleotide variant	NM_006187.4(OAS3):c.3218G>A (p.Arg1073Gln)	not specified [RCV004496483]	uncertain significance	12	112969721	112969721	Human		name
598194460	CV4001172	single nucleotide variant	NM_006187.4(OAS3):c.3167T>G (p.Leu1056Arg)	not specified [RCV005374719]	uncertain significance	12	112969670	112969670	Human		name

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