Spag5 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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117 records found for search term Spag5

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8585296	CV119879	single nucleotide variant	NM_006461.3(SPAG5):c.-483G>T	Lung cancer [RCV000100399]	uncertain significance	17	28599429	28599429	Human		name
41405120	CV982078	single nucleotide variant	NM_006461.4(SPAG5):c.3354+1G>A	not provided [RCV001812407]	uncertain significance	17	28578372	28578372	Human		name
401914160	CV2811167	single nucleotide variant	NM_006461.4(SPAG5):c.132C>T (p.Pro44=)	not provided [RCV003428197]	likely benign	17	28598555	28598555	Human		name
401903855	CV2811165	single nucleotide variant	NM_006461.4(SPAG5):c.765A>C (p.Ala255=)	not provided [RCV003419687]	likely benign	17	28592479	28592479	Human		name
598238719	CV3922586	single nucleotide variant	NM_006461.4(SPAG5):c.62C>A (p.Ser21Tyr)	not specified [RCV005275882]	uncertain significance	17	28598625	28598625	Human		name
155968889	CV2213237	single nucleotide variant	NM_006461.4(SPAG5):c.230A>G (p.Asp77Gly)	not specified [RCV004085459]	uncertain significance	17	28593014	28593014	Human		name
401935982	CV2811164	single nucleotide variant	NM_006461.4(SPAG5):c.1353G>A (p.Gln451=)	not provided [RCV003413178]	likely benign	17	28591782	28591782	Human		name
405788114	CV3329949	single nucleotide variant	NM_006461.4(SPAG5):c.131C>G (p.Pro44Arg)	not specified [RCV004459976]	uncertain significance	17	28598556	28598556	Human		name
405788138	CV3329954	single nucleotide variant	NM_006461.4(SPAG5):c.169G>A (p.Gly57Arg)	not specified [RCV004459981]	uncertain significance	17	28598518	28598518	Human		name
407510441	CV3481359	single nucleotide variant	NM_006461.4(SPAG5):c.232T>G (p.Leu78Val)	not specified [RCV004672734]	uncertain significance	17	28593012	28593012	Human		name
597757105	CV3600720	single nucleotide variant	NM_006461.4(SPAG5):c.211G>A (p.Val71Ile)	not specified [RCV004868561]	uncertain significance	17	28593033	28593033	Human		name
598248349	CV3922585	single nucleotide variant	NM_006461.4(SPAG5):c.295G>A (p.Glu99Lys)	not specified [RCV005277432]	uncertain significance	17	28592949	28592949	Human		name
598248364	CV3922588	single nucleotide variant	NM_006461.4(SPAG5):c.180A>T (p.Glu60Asp)	not specified [RCV005277434]	uncertain significance	17	28593064	28593064	Human		name
598248429	CV3922596	single nucleotide variant	NM_006461.4(SPAG5):c.199C>T (p.Pro67Ser)	not specified [RCV005277442]	uncertain significance	17	28593045	28593045	Human		name
15187095	CV771336	single nucleotide variant	NM_006461.4(SPAG5):c.2838G>A (p.Lys946=)	not provided [RCV000931556]	benign	17	28579797	28579797	Human		name
155970958	CV2262291	single nucleotide variant	NM_006461.4(SPAG5):c.443G>A (p.Arg148His)	not specified [RCV004128490]	likely benign	17	28592801	28592801	Human		name
156083548	CV2289601	single nucleotide variant	NM_006461.4(SPAG5):c.659G>C (p.Ser220Thr)	not specified [RCV004148526]	uncertain significance	17	28592585	28592585	Human		name
156210543	CV2314300	single nucleotide variant	NM_006461.4(SPAG5):c.517G>A (p.Glu173Lys)	not specified [RCV004166654]	uncertain significance	17	28592727	28592727	Human		name
156127065	CV2351093	single nucleotide variant	NM_006461.4(SPAG5):c.715G>A (p.Ala239Thr)	not specified [RCV004213955]	uncertain significance	17	28592529	28592529	Human		name
155902936	CV2356556	single nucleotide variant	NM_006461.4(SPAG5):c.524C>T (p.Ala175Val)	not specified [RCV004199465]	uncertain significance	17	28592720	28592720	Human		name
156167202	CV2399012	single nucleotide variant	NM_006461.4(SPAG5):c.644A>G (p.His215Arg)	not specified [RCV004245316]	uncertain significance	17	28592600	28592600	Human		name
401777514	CV2718230	single nucleotide variant	NM_006461.4(SPAG5):c.649T>C (p.Ser217Pro)	not specified [RCV004316222]	uncertain significance	17	28592595	28592595	Human		name
401890989	CV2768886	single nucleotide variant	NM_006461.4(SPAG5):c.842G>A (p.Arg281Lys)	not specified [RCV004346995]	uncertain significance	17	28592402	28592402	Human		name
401883708	CV2785742	single nucleotide variant	NM_006461.4(SPAG5):c.669T>G (p.Ser223Arg)	not specified [RCV004364997]	uncertain significance	17	28592575	28592575	Human		name
401914159	CV2811166	single nucleotide variant	NM_006461.4(SPAG5):c.686G>A (p.Arg229His)	not provided [RCV003428196]	likely benign	17	28592558	28592558	Human		name
405788199	CV3329967	single nucleotide variant	NM_006461.4(SPAG5):c.502G>A (p.Asp168Asn)	not specified [RCV004459994]	uncertain significance	17	28592742	28592742	Human		name
405788210	CV3329969	single nucleotide variant	NM_006461.4(SPAG5):c.536G>C (p.Gly179Ala)	not specified [RCV004459996]	uncertain significance	17	28592708	28592708	Human		name
405788215	CV3329970	single nucleotide variant	NM_006461.4(SPAG5):c.650C>T (p.Ser217Phe)	not specified [RCV004459997]	uncertain significance	17	28592594	28592594	Human		name
407510449	CV3481362	single nucleotide variant	NM_006461.4(SPAG5):c.560C>T (p.Ala187Val)	not specified [RCV004672737]	uncertain significance	17	28592684	28592684	Human		name
407510452	CV3481364	single nucleotide variant	NM_006461.4(SPAG5):c.658A>G (p.Ser220Gly)	not specified [RCV004672738]	uncertain significance	17	28592586	28592586	Human		name
407510458	CV3481366	single nucleotide variant	NM_006461.4(SPAG5):c.793C>A (p.Pro265Thr)	not specified [RCV004672740]	uncertain significance	17	28592451	28592451	Human		name
597757079	CV3600714	single nucleotide variant	NM_006461.4(SPAG5):c.317C>G (p.Pro106Arg)	not specified [RCV004868556]	uncertain significance	17	28592927	28592927	Human		name
597757085	CV3600715	single nucleotide variant	NM_006461.4(SPAG5):c.514G>A (p.Glu172Lys)	not specified [RCV004868557]	likely benign	17	28592730	28592730	Human		name
597741986	CV3600717	single nucleotide variant	NM_006461.4(SPAG5):c.313A>G (p.Ile105Val)	not specified [RCV004864984]	likely benign	17	28592931	28592931	Human		name
597757095	CV3600718	single nucleotide variant	NM_006461.4(SPAG5):c.686G>C (p.Arg229Pro)	not specified [RCV004868559]	likely benign	17	28592558	28592558	Human		name
597757100	CV3600719	single nucleotide variant	NM_006461.4(SPAG5):c.685C>T (p.Arg229Cys)	not specified [RCV004868560]	uncertain significance	17	28592559	28592559	Human		name
597757682	CV3600726	single nucleotide variant	NM_006461.4(SPAG5):c.776G>A (p.Arg259His)	not specified [RCV004868567]	uncertain significance	17	28592468	28592468	Human		name
598248371	CV3922589	single nucleotide variant	NM_006461.4(SPAG5):c.593C>T (p.Pro198Leu)	not specified [RCV005277435]	uncertain significance	17	28592651	28592651	Human		name
598248397	CV3922592	single nucleotide variant	NM_006461.4(SPAG5):c.533T>G (p.Met178Arg)	not specified [RCV005277438]	uncertain significance	17	28592711	28592711	Human		name
598238724	CV3922597	single nucleotide variant	NM_006461.4(SPAG5):c.935T>C (p.Leu312Pro)	not specified [RCV005275883]	likely benign	17	28592309	28592309	Human		name
598248448	CV3922600	single nucleotide variant	NM_006461.4(SPAG5):c.323T>C (p.Ile108Thr)	not specified [RCV005277445]	likely benign	17	28592921	28592921	Human		name
598248454	CV3922601	single nucleotide variant	NM_006461.4(SPAG5):c.763G>A (p.Ala255Thr)	not specified [RCV005277446]	uncertain significance	17	28592481	28592481	Human		name
15106445	CV715324	single nucleotide variant	NM_006461.4(SPAG5):c.368G>A (p.Gly123Asp)	not provided [RCV000960077]	likely benign	17	28592876	28592876	Human		name
155969925	CV2213406	single nucleotide variant	NM_006461.4(SPAG5):c.2440C>T (p.His814Tyr)	not specified [RCV004087386]	uncertain significance	17	28583959	28583959	Human		name
155973697	CV2239018	single nucleotide variant	NM_006461.4(SPAG5):c.2200A>G (p.Ser734Gly)	not specified [RCV004109900]	uncertain significance	17	28584442	28584442	Human		name
156297820	CV2240897	single nucleotide variant	NM_006461.4(SPAG5):c.1198A>G (p.Thr400Ala)	not specified [RCV004102182]	uncertain significance	17	28592046	28592046	Human		name
155993652	CV2252316	single nucleotide variant	NM_006461.4(SPAG5):c.2595G>C (p.Glu865Asp)	not specified [RCV004116174]	uncertain significance	17	28583601	28583601	Human		name
155947366	CV2262634	single nucleotide variant	NM_006461.4(SPAG5):c.2635G>A (p.Glu879Lys)	not specified [RCV004130832]	uncertain significance	17	28583561	28583561	Human		name
155916078	CV2281894	single nucleotide variant	NM_006461.4(SPAG5):c.1249C>G (p.Gln417Glu)	not specified [RCV004138674]	uncertain significance	17	28591995	28591995	Human		name
155985772	CV2282406	single nucleotide variant	NM_006461.4(SPAG5):c.2093C>T (p.Ser698Phe)	not specified [RCV004133220]	uncertain significance	17	28584720	28584720	Human		name
156102293	CV2291479	single nucleotide variant	NM_006461.4(SPAG5):c.1613G>A (p.Arg538His)	not specified [RCV004155798]	likely benign	17	28585991	28585991	Human		name
155937173	CV2376333	single nucleotide variant	NM_006461.4(SPAG5):c.1564C>G (p.Leu522Val)	not specified [RCV004222593]	uncertain significance	17	28586131	28586131	Human		name
156095809	CV2378050	single nucleotide variant	NM_006461.4(SPAG5):c.1397C>T (p.Thr466Ile)	not specified [RCV004232611]	uncertain significance	17	28591738	28591738	Human		name
155938435	CV2380746	single nucleotide variant	NM_006461.4(SPAG5):c.2023C>G (p.Gln675Glu)	not specified [RCV004218314]	uncertain significance	17	28585146	28585146	Human		name
156062956	CV2392178	single nucleotide variant	NM_006461.4(SPAG5):c.1078C>T (p.Arg360Cys)	not specified [RCV004238067]	uncertain significance	17	28592166	28592166	Human		name
156188157	CV2395373	single nucleotide variant	NM_006461.4(SPAG5):c.2783C>A (p.Ala928Glu)	not specified [RCV004239464]	uncertain significance	17	28580023	28580023	Human		name
329376091	CV2431726	single nucleotide variant	NM_006461.4(SPAG5):c.1060G>C (p.Val354Leu)	not specified [RCV004248888]	uncertain significance	17	28592184	28592184	Human		name
329368661	CV2453256	single nucleotide variant	NM_006461.4(SPAG5):c.2837A>G (p.Lys946Arg)	not specified [RCV004266897]	uncertain significance	17	28579798	28579798	Human		name
401740535	CV2679747	single nucleotide variant	NM_006461.4(SPAG5):c.1282G>A (p.Ala428Thr)	not specified [RCV004282212]	uncertain significance	17	28591853	28591853	Human		name
401762680	CV2714235	single nucleotide variant	NM_006461.4(SPAG5):c.2006T>C (p.Leu669Pro)	not specified [RCV004317460]	uncertain significance	17	28585163	28585163	Human		name
401769458	CV2735066	single nucleotide variant	NM_006461.4(SPAG5):c.2886G>C (p.Glu962Asp)	not specified [RCV004333763]	uncertain significance	17	28579484	28579484	Human		name
401864780	CV2761042	single nucleotide variant	NM_006461.4(SPAG5):c.1349G>T (p.Arg450Leu)	not specified [RCV004338709]	uncertain significance	17	28591786	28591786	Human		name
401892739	CV2761948	single nucleotide variant	NM_006461.4(SPAG5):c.1774G>A (p.Ala592Thr)	not specified [RCV004339572]	uncertain significance	17	28585620	28585620	Human		name
401876868	CV2767744	single nucleotide variant	NM_006461.4(SPAG5):c.2168G>A (p.Arg723Gln)	not specified [RCV004345873]	likely benign	17	28584474	28584474	Human		name
405788109	CV3329948	single nucleotide variant	NM_006461.4(SPAG5):c.1108C>T (p.Arg370Trp)	not specified [RCV004459975]	uncertain significance	17	28592136	28592136	Human		name
405788119	CV3329950	single nucleotide variant	NM_006461.4(SPAG5):c.1327G>C (p.Val443Leu)	not specified [RCV004459977]	uncertain significance	17	28591808	28591808	Human		name
405788124	CV3329951	single nucleotide variant	NM_006461.4(SPAG5):c.1343T>A (p.Leu448His)	not specified [RCV004459978]	uncertain significance	17	28591792	28591792	Human		name
405788129	CV3329952	single nucleotide variant	NM_006461.4(SPAG5):c.1470C>A (p.Ser490Arg)	not specified [RCV004459979]	uncertain significance	17	28586467	28586467	Human		name
405788133	CV3329953	single nucleotide variant	NM_006461.4(SPAG5):c.1529T>C (p.Ile510Thr)	not specified [RCV004459980]	uncertain significance	17	28586166	28586166	Human		name
405788144	CV3329955	single nucleotide variant	NM_006461.4(SPAG5):c.1723C>T (p.Leu575Phe)	not specified [RCV004459982]	uncertain significance	17	28585881	28585881	Human		name
405788148	CV3329956	single nucleotide variant	NM_006461.4(SPAG5):c.1826T>C (p.Phe609Ser)	not specified [RCV004459983]	uncertain significance	17	28585568	28585568	Human		name
405788158	CV3329958	single nucleotide variant	NM_006461.4(SPAG5):c.2380A>G (p.Lys794Glu)	not specified [RCV004459985]	uncertain significance	17	28584182	28584182	Human		name
405788161	CV3329959	single nucleotide variant	NM_006461.4(SPAG5):c.2599A>C (p.Thr867Pro)	not specified [RCV004459986]	uncertain significance	17	28583597	28583597	Human		name
405788166	CV3329960	single nucleotide variant	NM_006461.4(SPAG5):c.2926A>G (p.Met976Val)	not specified [RCV004459987]	uncertain significance	17	28579444	28579444	Human		name
405788171	CV3329961	single nucleotide variant	NM_006461.4(SPAG5):c.2983A>T (p.Ile995Phe)	not specified [RCV004459988]	uncertain significance	17	28579387	28579387	Human		name
407510435	CV3481357	single nucleotide variant	NM_006461.4(SPAG5):c.2194A>G (p.Met732Val)	not specified [RCV004672732]	uncertain significance	17	28584448	28584448	Human		name
407510438	CV3481358	single nucleotide variant	NM_006461.4(SPAG5):c.2362C>A (p.Gln788Lys)	not specified [RCV004672733]	uncertain significance	17	28584200	28584200	Human		name
407510443	CV3481360	single nucleotide variant	NM_006461.4(SPAG5):c.1907G>A (p.Ser636Asn)	not specified [RCV004672735]	uncertain significance	17	28585365	28585365	Human		name
407510446	CV3481361	single nucleotide variant	NM_006461.4(SPAG5):c.2167C>T (p.Arg723Trp)	not specified [RCV004672736]	uncertain significance	17	28584475	28584475	Human		name
407510455	CV3481365	single nucleotide variant	NM_006461.4(SPAG5):c.2054A>C (p.Glu685Ala)	not specified [RCV004672739]	uncertain significance	17	28585115	28585115	Human		name
407510464	CV3481368	single nucleotide variant	NM_006461.4(SPAG5):c.2149C>T (p.Arg717Cys)	not specified [RCV004672742]	uncertain significance	17	28584664	28584664	Human		name
407510466	CV3481369	single nucleotide variant	NM_006461.4(SPAG5):c.2500C>T (p.Arg834Cys)	not specified [RCV004672743]	uncertain significance	17	28583899	28583899	Human		name
597757090	CV3600716	single nucleotide variant	NM_006461.4(SPAG5):c.2563A>G (p.Thr855Ala)	not specified [RCV004868558]	uncertain significance	17	28583633	28583633	Human		name
597757110	CV3600721	single nucleotide variant	NM_006461.4(SPAG5):c.2693A>G (p.Gln898Arg)	not specified [RCV004868562]	uncertain significance	17	28580113	28580113	Human		name
597757116	CV3600722	single nucleotide variant	NM_006461.4(SPAG5):c.1100C>T (p.Ser367Leu)	not specified [RCV004868563]	uncertain significance	17	28592144	28592144	Human		name
597757121	CV3600723	single nucleotide variant	NM_006461.4(SPAG5):c.1082A>G (p.Gln361Arg)	not specified [RCV004868564]	uncertain significance	17	28592162	28592162	Human		name
597757131	CV3600725	single nucleotide variant	NM_006461.4(SPAG5):c.1349G>A (p.Arg450His)	not specified [RCV004868566]	likely benign	17	28591786	28591786	Human		name
597741990	CV3600727	single nucleotide variant	NM_006461.4(SPAG5):c.1877A>C (p.Lys626Thr)	not specified [RCV004864985]	uncertain significance	17	28585395	28585395	Human		name
598238714	CV3922584	single nucleotide variant	NM_006461.4(SPAG5):c.1348C>T (p.Arg450Cys)	not specified [RCV005275881]	uncertain significance	17	28591787	28591787	Human		name
598248354	CV3922587	single nucleotide variant	NM_006461.4(SPAG5):c.1820G>A (p.Arg607Gln)	not specified [RCV005277433]	likely benign	17	28585574	28585574	Human		name
598248380	CV3922590	single nucleotide variant	NM_006461.4(SPAG5):c.2494C>T (p.Arg832Trp)	not specified [RCV005277436]	uncertain significance	17	28583905	28583905	Human		name
598248390	CV3922591	single nucleotide variant	NM_006461.4(SPAG5):c.1487C>T (p.Ala496Val)	not specified [RCV005277437]	uncertain significance	17	28586450	28586450	Human		name
598248413	CV3922594	single nucleotide variant	NM_006461.4(SPAG5):c.2348C>A (p.Ala783Glu)	not specified [RCV005277440]	uncertain significance	17	28584214	28584214	Human		name
598248421	CV3922595	single nucleotide variant	NM_006461.4(SPAG5):c.1625T>C (p.Leu542Ser)	not specified [RCV005277441]	uncertain significance	17	28585979	28585979	Human		name
598248435	CV3922598	single nucleotide variant	NM_006461.4(SPAG5):c.2951G>T (p.Cys984Phe)	not specified [RCV005277443]	uncertain significance	17	28579419	28579419	Human		name
598248444	CV3922599	single nucleotide variant	NM_006461.4(SPAG5):c.2624G>A (p.Gly875Glu)	not specified [RCV005277444]	uncertain significance	17	28583572	28583572	Human		name
156326822	CV2219698	single nucleotide variant	NM_006461.4(SPAG5):c.3371T>C (p.Val1124Ala)	not specified [RCV004095409]	uncertain significance	17	28578276	28578276	Human		name
156049283	CV2315837	single nucleotide variant	NM_006461.4(SPAG5):c.3103T>C (p.Cys1035Arg)	not specified [RCV004171616]	uncertain significance	17	28579155	28579155	Human		name
155985852	CV2345429	single nucleotide variant	NM_006461.4(SPAG5):c.3320A>G (p.Asn1107Ser)	not specified [RCV004198204]	likely benign	17	28578407	28578407	Human		name
156344426	CV2364278	single nucleotide variant	NM_006461.4(SPAG5):c.3238C>T (p.Arg1080Trp)	not specified [RCV004223504]	uncertain significance	17	28578489	28578489	Human		name
329382055	CV2424313	single nucleotide variant	NM_006461.4(SPAG5):c.3539G>C (p.Arg1180Thr)	not specified [RCV004252220]	uncertain significance	17	28577742	28577742	Human		name
329379424	CV2443405	single nucleotide variant	NM_006461.4(SPAG5):c.3310A>G (p.Met1104Val)	not specified [RCV004262248]	likely benign	17	28578417	28578417	Human		name
401761240	CV2689077	single nucleotide variant	NM_006461.4(SPAG5):c.3143T>C (p.Ile1048Thr)	not specified [RCV004305845]	uncertain significance	17	28578727	28578727	Human		name
401884934	CV2771071	single nucleotide variant	NM_006461.4(SPAG5):c.3526C>G (p.Pro1176Ala)	not specified [RCV004346079]	uncertain significance	17	28577755	28577755	Human		name
405788175	CV3329962	single nucleotide variant	NM_006461.4(SPAG5):c.3145C>A (p.Gln1049Lys)	not specified [RCV004459989]	uncertain significance	17	28578725	28578725	Human		name
405788179	CV3329963	single nucleotide variant	NM_006461.4(SPAG5):c.3176T>C (p.Ile1059Thr)	not specified [RCV004459990]	uncertain significance	17	28578694	28578694	Human		name
405788184	CV3329964	single nucleotide variant	NM_006461.4(SPAG5):c.3226A>G (p.Thr1076Ala)	not specified [RCV004459991]	uncertain significance	17	28578501	28578501	Human		name
405788188	CV3329965	single nucleotide variant	NM_006461.4(SPAG5):c.3409A>G (p.Met1137Val)	not specified [RCV004459992]	uncertain significance	17	28578238	28578238	Human		name
405788193	CV3329966	single nucleotide variant	NM_006461.4(SPAG5):c.3469G>A (p.Glu1157Lys)	not specified [RCV004459993]	uncertain significance	17	28578051	28578051	Human		name
407525443	CV3481363	single nucleotide variant	NM_006461.4(SPAG5):c.3370G>T (p.Val1124Leu)	not specified [RCV004679260]	uncertain significance	17	28578277	28578277	Human		name
407510461	CV3481367	single nucleotide variant	NM_006461.4(SPAG5):c.3010G>A (p.Glu1004Lys)	not specified [RCV004672741]	uncertain significance	17	28579248	28579248	Human		name
597757074	CV3600713	single nucleotide variant	NM_006461.4(SPAG5):c.3229C>T (p.Arg1077Cys)	not specified [RCV004868555]	uncertain significance	17	28578498	28578498	Human		name
597757126	CV3600724	single nucleotide variant	NM_006461.4(SPAG5):c.3340T>C (p.Trp1114Arg)	not specified [RCV004868565]	uncertain significance	17	28578387	28578387	Human		name
597741994	CV3600728	single nucleotide variant	NM_006461.4(SPAG5):c.3079A>T (p.Ile1027Leu)	not specified [RCV004864986]	uncertain significance	17	28579179	28579179	Human		name
597757690	CV3600729	single nucleotide variant	NM_006461.4(SPAG5):c.3373A>G (p.Met1125Val)	not specified [RCV004868568]	uncertain significance	17	28578274	28578274	Human		name
598248406	CV3922593	single nucleotide variant	NM_006461.4(SPAG5):c.3135G>C (p.Gln1045His)	not specified [RCV005277439]	uncertain significance	17	28578735	28578735	Human		name
41405122	CV982077	single nucleotide variant	NM_006461.4(SPAG5):c.3386T>A (p.Met1129Lys)	not provided [RCV001812409]\|not specified [RCV004671311]	uncertain significance	17	28578261	28578261	Human		name

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