Spag8 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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69 records found for search term Spag8

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156363426	CV2329879	single nucleotide variant	NM_001039592.2(SPAG8):c.8C>T (p.Thr3Ile)	not specified [RCV004183337]	uncertain significance	9	35812140	35812140	Human		name
15203274	CV751707	single nucleotide variant	NM_001039592.2(SPAG8):c.30G>C (p.Ser10=)	not provided [RCV000913822]	likely benign	9	35812118	35812118	Human		name
156039581	CV2261224	single nucleotide variant	NM_001039592.2(SPAG8):c.14A>C (p.Glu5Ala)	not specified [RCV004128101]	uncertain significance	9	35812134	35812134	Human		name
15146205	CV711968	single nucleotide variant	NM_001039592.2(SPAG8):c.294G>A (p.Ala98=)	not provided [RCV000967126]	benign	9	35811752	35811752	Human		name
15118380	CV711969	single nucleotide variant	NM_001039592.2(SPAG8):c.159G>A (p.Ala53=)	not provided [RCV000962367]	benign	9	35811887	35811887	Human		name
156388344	CV2231798	single nucleotide variant	NM_172312.2(SPAG8):c.1413A>T (p.Glu471Asp)	not specified [RCV004098608]	uncertain significance	9	35808266	35808266	Human		name
156292907	CV2321256	single nucleotide variant	NM_172312.2(SPAG8):c.1442A>G (p.Asn481Ser)	not specified [RCV004175370]	uncertain significance	9	35808237	35808237	Human		name
155975278	CV2342650	single nucleotide variant	NM_001039592.2(SPAG8):c.74G>A (p.Gly25Glu)	not specified [RCV004196735]	uncertain significance	9	35811972	35811972	Human		name
156337201	CV2343021	single nucleotide variant	NM_001039592.2(SPAG8):c.64A>G (p.Ser22Gly)	not specified [RCV004192623]	uncertain significance	9	35811982	35811982	Human		name
405788260	CV3329979	single nucleotide variant	NM_172312.2(SPAG8):c.1385A>G (p.Tyr462Cys)	not specified [RCV004460006]	uncertain significance	9	35808294	35808294	Human		name
407451131	CV3481384	single nucleotide variant	NM_172312.2(SPAG8):c.1417C>T (p.Pro473Ser)	not specified [RCV004672756]	uncertain significance	9	35808262	35808262	Human		name
597688626	CV3600740	single nucleotide variant	NM_172312.2(SPAG8):c.1463T>C (p.Met488Thr)	not specified [RCV004868577]	uncertain significance	9	35808216	35808216	Human		name
597687812	CV3600745	single nucleotide variant	NM_172312.2(SPAG8):c.1313C>G (p.Thr438Ser)	not specified [RCV004864989]	uncertain significance	9	35809463	35809463	Human		name
597742008	CV3600748	single nucleotide variant	NM_001039592.2(SPAG8):c.68C>T (p.Ser23Phe)	not specified [RCV004864990]	uncertain significance	9	35811978	35811978	Human		name
597757239	CV3600752	single nucleotide variant	NM_001039592.2(SPAG8):c.29C>T (p.Ser10Leu)	not specified [RCV004868587]	uncertain significance	9	35812119	35812119	Human		name
598248503	CV3922608	single nucleotide variant	NM_172312.2(SPAG8):c.1273C>T (p.Pro425Ser)	not specified [RCV005277453]	uncertain significance	9	35809503	35809503	Human		name
15145061	CV692673	single nucleotide variant	NM_172312.2(SPAG8):c.1402G>A (p.Gly468Arg)	not provided [RCV000878320]	benign	9	35808277	35808277	Human		name
15101324	CV701001	single nucleotide variant	NM_001039592.2(SPAG8):c.828G>A (p.Pro276=)	not provided [RCV000959065]	benign	9	35811218	35811218	Human		name
8689424	CV97512	single nucleotide variant	NM_001039592.2(SPAG8):c.618C>T (p.Asp206=)	not provided [RCV000122591]	uncertain significance	9	35811428	35811428	Human		name
156298777	CV2240995	single nucleotide variant	NM_001039592.2(SPAG8):c.293C>G (p.Ala98Gly)	not specified [RCV004102263]	uncertain significance	9	35811753	35811753	Human		name
401774340	CV2727809	single nucleotide variant	NM_001039592.2(SPAG8):c.133G>C (p.Ala45Pro)	not specified [RCV004323834]	uncertain significance	9	35811913	35811913	Human		name
405788249	CV3329977	single nucleotide variant	NM_001039592.2(SPAG8):c.1086T>C (p.Cys362=)	not specified [RCV004460004]	likely benign	9	35810553	35810553	Human		name
405788263	CV3329980	single nucleotide variant	NM_001039592.2(SPAG8):c.233C>T (p.Ala78Val)	not specified [RCV004460007]	uncertain significance	9	35811813	35811813	Human		name
405788269	CV3329981	single nucleotide variant	NM_001039592.2(SPAG8):c.239G>C (p.Cys80Ser)	not specified [RCV004460008]	uncertain significance	9	35811807	35811807	Human		name
407510508	CV3481385	single nucleotide variant	NM_001039592.2(SPAG8):c.169G>A (p.Ala57Thr)	not specified [RCV004672757]	uncertain significance	9	35811877	35811877	Human		name
598248496	CV3922607	single nucleotide variant	NM_001039592.2(SPAG8):c.164C>T (p.Ala55Val)	not specified [RCV005277452]	uncertain significance	9	35811882	35811882	Human		name
156379442	CV2214788	single nucleotide variant	NM_001039592.2(SPAG8):c.670C>T (p.Arg224Trp)	not specified [RCV004090592]	uncertain significance	9	35811376	35811376	Human		name
156064678	CV2229015	single nucleotide variant	NM_001039592.2(SPAG8):c.584C>T (p.Pro195Leu)	not specified [RCV004098799]	uncertain significance	9	35811462	35811462	Human		name
156243173	CV2231494	single nucleotide variant	NM_001039592.2(SPAG8):c.900G>A (p.Met300Ile)	not specified [RCV004096562]	uncertain significance	9	35811022	35811022	Human		name
156229465	CV2267663	single nucleotide variant	NM_001039592.2(SPAG8):c.346G>T (p.Val116Phe)	not specified [RCV004134213]	uncertain significance	9	35811700	35811700	Human		name
156033018	CV2275072	single nucleotide variant	NM_001039592.2(SPAG8):c.689C>A (p.Ser230Tyr)	not specified [RCV004136891]	uncertain significance	9	35811357	35811357	Human		name
156172423	CV2293338	single nucleotide variant	NM_001039592.2(SPAG8):c.989C>A (p.Thr330Asn)	not specified [RCV004150820]	uncertain significance	9	35810933	35810933	Human		name
156265843	CV2299301	single nucleotide variant	NM_001039592.2(SPAG8):c.830G>A (p.Arg277Gln)	not specified [RCV004152622]	uncertain significance	9	35811216	35811216	Human		name
156149204	CV2359471	single nucleotide variant	NM_001039592.2(SPAG8):c.706C>T (p.Pro236Ser)	not specified [RCV004214788]	uncertain significance	9	35811340	35811340	Human		name
156102775	CV2363216	single nucleotide variant	NM_001039592.2(SPAG8):c.989C>G (p.Thr330Ser)	not specified [RCV004213781]	uncertain significance	9	35810933	35810933	Human		name
156188696	CV2375409	single nucleotide variant	NM_001039592.2(SPAG8):c.593G>C (p.Gly198Ala)	not specified [RCV004232803]	uncertain significance	9	35811453	35811453	Human		name
156347246	CV2375410	single nucleotide variant	NM_001039592.2(SPAG8):c.756A>C (p.Glu252Asp)	not specified [RCV004232804]	uncertain significance	9	35811290	35811290	Human		name
329379458	CV2443419	single nucleotide variant	NM_001039592.2(SPAG8):c.313A>T (p.Asn105Tyr)	not specified [RCV004262260]	uncertain significance	9	35811733	35811733	Human		name
329395870	CV2463027	single nucleotide variant	NM_001039592.2(SPAG8):c.395G>C (p.Ser132Thr)	not specified [RCV004272846]	uncertain significance	9	35811651	35811651	Human		name
401746456	CV2695573	single nucleotide variant	NM_001039592.2(SPAG8):c.925T>G (p.Phe309Val)	not specified [RCV004305743]	uncertain significance	9	35810997	35810997	Human		name
405788273	CV3329982	single nucleotide variant	NM_001039592.2(SPAG8):c.392A>G (p.His131Arg)	not specified [RCV004460009]	uncertain significance	9	35811654	35811654	Human		name
405788278	CV3329983	single nucleotide variant	NM_001039592.2(SPAG8):c.548C>G (p.Ser183Cys)	not specified [RCV004460010]	uncertain significance	9	35811498	35811498	Human		name
405788282	CV3329984	single nucleotide variant	NM_001039592.2(SPAG8):c.574C>G (p.His192Asp)	not specified [RCV004460011]	uncertain significance	9	35811472	35811472	Human		name
405788286	CV3329985	single nucleotide variant	NM_001039592.2(SPAG8):c.911C>T (p.Ser304Phe)	not specified [RCV004460012]	uncertain significance	9	35811011	35811011	Human		name
407510505	CV3481383	single nucleotide variant	NM_001039592.2(SPAG8):c.728C>G (p.Pro243Arg)	not specified [RCV004672755]	uncertain significance	9	35811318	35811318	Human		name
407510511	CV3481386	single nucleotide variant	NM_001039592.2(SPAG8):c.487C>T (p.Pro163Ser)	not specified [RCV004672758]	uncertain significance	9	35811559	35811559	Human		name
597742003	CV3600739	single nucleotide variant	NM_001039592.2(SPAG8):c.443G>A (p.Gly148Asp)	not specified [RCV004864988]	uncertain significance	9	35811603	35811603	Human		name
597757194	CV3600742	single nucleotide variant	NM_001039592.2(SPAG8):c.955A>G (p.Met319Val)	not specified [RCV004868579]	uncertain significance	9	35810967	35810967	Human		name
597757200	CV3600743	single nucleotide variant	NM_001039592.2(SPAG8):c.941G>A (p.Arg314Gln)	not specified [RCV004868580]	likely benign	9	35810981	35810981	Human		name
597757228	CV3600750	single nucleotide variant	NM_001039592.2(SPAG8):c.352G>A (p.Val118Ile)	not specified [RCV004868585]	uncertain significance	9	35811694	35811694	Human		name
597757234	CV3600751	single nucleotide variant	NM_001039592.2(SPAG8):c.508G>A (p.Gly170Ser)	not specified [RCV004868586]	uncertain significance	9	35811538	35811538	Human		name
598248489	CV3922606	single nucleotide variant	NM_001039592.2(SPAG8):c.918T>G (p.Ser306Arg)	not specified [RCV005277451]	uncertain significance	9	35811004	35811004	Human		name
15158903	CV701002	single nucleotide variant	NM_001039592.2(SPAG8):c.598G>A (p.Gly200Ser)	not provided [RCV000947166]	benign	9	35811448	35811448	Human		name
15107064	CV723567	single nucleotide variant	NM_001039592.2(SPAG8):c.328A>G (p.Ser110Gly)	not provided [RCV000893402]	benign	9	35811718	35811718	Human		name
15171124	CV737130	single nucleotide variant	NM_001039592.2(SPAG8):c.928C>T (p.Arg310Ter)	not provided [RCV000905403]	benign	9	35810994	35810994	Human		name
156330879	CV2210717	single nucleotide variant	NM_001039592.2(SPAG8):c.1160G>A (p.Arg387Gln)	not specified [RCV004083856]	uncertain significance	9	35810479	35810479	Human		name
156331947	CV2218237	single nucleotide variant	NM_001039592.2(SPAG8):c.1037G>A (p.Arg346Gln)	not specified [RCV004088437]	uncertain significance	9	35810885	35810885	Human		name
156156436	CV2266215	single nucleotide variant	NM_001039592.2(SPAG8):c.1031C>T (p.Pro344Leu)	not specified [RCV004128785]	uncertain significance	9	35810891	35810891	Human		name
156396786	CV2330270	single nucleotide variant	NM_001039592.2(SPAG8):c.1180G>A (p.Gly394Arg)	not specified [RCV004187719]	uncertain significance	9	35810459	35810459	Human		name
156105912	CV2361353	single nucleotide variant	NM_001039592.2(SPAG8):c.1151A>G (p.His384Arg)	not specified [RCV004218556]	uncertain significance	9	35810488	35810488	Human		name
405788255	CV3329978	single nucleotide variant	NM_001039592.2(SPAG8):c.1217A>C (p.Gln406Pro)	not specified [RCV004460005]	uncertain significance	9	35810293	35810293	Human		name
407510502	CV3481382	single nucleotide variant	NM_001039592.2(SPAG8):c.1046G>A (p.Arg349His)	not specified [RCV004672754]	uncertain significance	9	35810676	35810676	Human		name
597757189	CV3600741	single nucleotide variant	NM_001039592.2(SPAG8):c.1255C>G (p.Gln419Glu)	not specified [RCV004868578]	uncertain significance	9	35810255	35810255	Human		name
597757206	CV3600744	single nucleotide variant	NM_001039592.2(SPAG8):c.1214G>A (p.Arg405His)	not specified [RCV004868581]	uncertain significance	9	35810296	35810296	Human		name
597757211	CV3600746	single nucleotide variant	NM_001039592.2(SPAG8):c.1172C>A (p.Ala391Glu)	not specified [RCV004868582]	uncertain significance	9	35810467	35810467	Human		name
597757216	CV3600747	single nucleotide variant	NM_001039592.2(SPAG8):c.1213C>T (p.Arg405Cys)	not specified [RCV004868583]	uncertain significance	9	35810297	35810297	Human		name
597757222	CV3600749	single nucleotide variant	NM_001039592.2(SPAG8):c.1021G>A (p.Val341Ile)	not specified [RCV004868584]	uncertain significance	9	35810901	35810901	Human		name
597757245	CV3600753	single nucleotide variant	NM_001039592.2(SPAG8):c.1206C>A (p.His402Gln)	not specified [RCV004868588]	uncertain significance	9	35810304	35810304	Human		name
15107059	CV723566	single nucleotide variant	NM_001039592.2(SPAG8):c.1262C>T (p.Pro421Leu)	not provided [RCV000893401]	benign	9	35810248	35810248	Human		name

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