Stard8 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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113 records found for search term Stard8

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8587588	CV122219	single nucleotide variant	NM_014725.4(STARD8):c.-79-10343C>T	Lung cancer [RCV000102739]	uncertain significance	X	68702571	68702571	Human		name
401740367	CV2684340	single nucleotide variant	NM_001142503.3(STARD8):c.5C>G (p.Pro2Arg)	not specified [RCV004288989]	uncertain significance	X	68647887	68647887	Human		name
597682831	CV3618426	single nucleotide variant	NM_001142503.3(STARD8):c.25T>G (p.Ser9Ala)	not specified [RCV004857686]	likely benign	X	68647907	68647907	Human		name
401927234	CV2829176	single nucleotide variant	NM_001142503.3(STARD8):c.429C>T (p.Thr143=)	not provided [RCV003438456]	likely benign	X	68717343	68717343	Human		name
597682861	CV3618432	single nucleotide variant	NM_001142503.3(STARD8):c.72G>T (p.Lys24Asn)	not specified [RCV004857689]	uncertain significance	X	68665525	68665525	Human		name
598250590	CV3919434	single nucleotide variant	NM_001142503.3(STARD8):c.85G>A (p.Glu29Lys)	not specified [RCV005277737]	uncertain significance	X	68712919	68712919	Human		name
156299129	CV2244700	single nucleotide variant	NM_001142503.3(STARD8):c.280C>A (p.His94Asn)	not specified [RCV004102701]	uncertain significance	X	68716414	68716414	Human		name
401741606	CV2676485	single nucleotide variant	NM_001142503.3(STARD8):c.196G>A (p.Gly66Ser)	not specified [RCV004288684]	likely benign	X	68715338	68715338	Human		name
401927239	CV2829180	single nucleotide variant	NM_001142503.3(STARD8):c.1314T>C (p.Ala438=)	not provided [RCV003438460]	likely benign	X	68718228	68718228	Human		name
401927244	CV2829184	single nucleotide variant	NM_001142503.3(STARD8):c.1983G>A (p.Thr661=)	not provided [RCV003438464]	likely benign	X	68720357	68720357	Human		name
407495859	CV3485330	single nucleotide variant	NM_001142503.3(STARD8):c.157T>C (p.Ser53Pro)	not specified [RCV004667978]	uncertain significance	X	68715299	68715299	Human		name
596947772	CV3547355	single nucleotide variant	NM_001142503.3(STARD8):c.1983G>C (p.Thr661=)	not provided [RCV004811659]	likely benign	X	68720357	68720357	Human		name
597746845	CV3618420	single nucleotide variant	NM_001142503.3(STARD8):c.263C>T (p.Ser88Leu)	not specified [RCV004865953]	uncertain significance	X	68716397	68716397	Human		name
15194319	CV706292	single nucleotide variant	NM_001142503.3(STARD8):c.2488A>C (p.Arg830=)	not provided [RCV000955613]	benign	X	68722075	68722075	Human		name
15164936	CV729685	single nucleotide variant	NM_001142503.3(STARD8):c.1164A>G (p.Leu388=)	not provided [RCV000882304]	benign	X	68718078	68718078	Human		name
15106066	CV786891	single nucleotide variant	NM_001142503.3(STARD8):c.2409G>A (p.Ala803=)	not provided [RCV000976563]	benign	X	68721696	68721696	Human		name
156323767	CV2201851	single nucleotide variant	NM_001142503.3(STARD8):c.400G>A (p.Ala134Thr)	not specified [RCV004082279]	uncertain significance	X	68717314	68717314	Human		name
156068979	CV2237091	single nucleotide variant	NM_001142503.3(STARD8):c.901G>T (p.Val301Phe)	not specified [RCV004114849]	uncertain significance	X	68717815	68717815	Human		name
156286885	CV2288346	single nucleotide variant	NM_001142503.3(STARD8):c.619C>T (p.Arg207Cys)	not specified [RCV004150115]	uncertain significance	X	68717533	68717533	Human		name
155969145	CV2339389	single nucleotide variant	NM_001142503.3(STARD8):c.550C>T (p.Arg184Trp)	not specified [RCV004191611]	uncertain significance	X	68717464	68717464	Human		name
155901635	CV2345845	single nucleotide variant	NM_001142503.3(STARD8):c.341A>G (p.His114Arg)	not specified [RCV004198889]	uncertain significance	X	68717255	68717255	Human		name
329397723	CV2463954	single nucleotide variant	NM_001142503.3(STARD8):c.880C>T (p.Arg294Trp)	not specified [RCV004273673]	uncertain significance	X	68717794	68717794	Human		name
329381905	CV2467413	single nucleotide variant	NM_001142503.3(STARD8):c.321G>T (p.Glu107Asp)	not specified [RCV004287030]	uncertain significance	X	68717235	68717235	Human		name
329393675	CV2472076	single nucleotide variant	NM_001142503.3(STARD8):c.920C>T (p.Pro307Leu)	not specified [RCV004283215]	uncertain significance	X	68717834	68717834	Human		name
401863701	CV2773182	single nucleotide variant	NM_001142503.3(STARD8):c.881G>A (p.Arg294Gln)	not specified [RCV004351907]	uncertain significance	X	68717795	68717795	Human		name
401890805	CV2778361	single nucleotide variant	NM_001142503.3(STARD8):c.784T>C (p.Trp262Arg)	not specified [RCV004344049]	likely benign	X	68717698	68717698	Human		name
401876507	CV2782944	single nucleotide variant	NM_001142503.3(STARD8):c.583G>A (p.Gly195Ser)	not specified [RCV004361739]	uncertain significance	X	68717497	68717497	Human		name
401927235	CV2829177	single nucleotide variant	NM_001142503.3(STARD8):c.614G>A (p.Arg205His)	not provided [RCV003438457]	likely benign	X	68717528	68717528	Human		name
401927237	CV2829178	single nucleotide variant	NM_001142503.3(STARD8):c.653G>A (p.Arg218Gln)	not provided [RCV003438458]	likely benign	X	68717567	68717567	Human		name
401927238	CV2829179	single nucleotide variant	NM_001142503.3(STARD8):c.746G>A (p.Arg249His)	not provided [RCV003438459]\|not specified [RCV004673892]	likely benign\|uncertain significance	X	68717660	68717660	Human		name
405738839	CV3323805	single nucleotide variant	NM_001142503.3(STARD8):c.298A>G (p.Asn100Asp)	not specified [RCV004465390]	uncertain significance	X	68717212	68717212	Human		name
405738849	CV3323806	single nucleotide variant	NM_001142503.3(STARD8):c.385T>A (p.Ser129Thr)	not specified [RCV004465391]	uncertain significance	X	68717299	68717299	Human		name
405738856	CV3323807	single nucleotide variant	NM_001142503.3(STARD8):c.611A>G (p.His204Arg)	not specified [RCV004465392]	uncertain significance	X	68717525	68717525	Human		name
405738864	CV3323808	single nucleotide variant	NM_001142503.3(STARD8):c.620G>A (p.Arg207His)	not specified [RCV004465393]	uncertain significance	X	68717534	68717534	Human		name
405740380	CV3323809	single nucleotide variant	NM_001142503.3(STARD8):c.745C>T (p.Arg249Cys)	not specified [RCV004465394]	uncertain significance	X	68717659	68717659	Human		name
405738887	CV3323811	single nucleotide variant	NM_001142503.3(STARD8):c.935G>A (p.Arg312His)	not specified [RCV004465396]	uncertain significance	X	68717849	68717849	Human		name
407530084	CV3485322	single nucleotide variant	NM_001142503.3(STARD8):c.791C>A (p.Ala264Asp)	not specified [RCV004681625]	uncertain significance	X	68717705	68717705	Human		name
407495831	CV3485324	single nucleotide variant	NM_001142503.3(STARD8):c.790G>A (p.Ala264Thr)	not specified [RCV004667972]	uncertain significance	X	68717704	68717704	Human		name
407495850	CV3485328	single nucleotide variant	NM_001142503.3(STARD8):c.333C>G (p.Ile111Met)	not specified [RCV004667976]	uncertain significance	X	68717247	68717247	Human		name
407495864	CV3485331	single nucleotide variant	NM_001142503.3(STARD8):c.607C>T (p.Arg203Cys)	not specified [RCV004667979]	uncertain significance	X	68717521	68717521	Human		name
597746849	CV3618421	single nucleotide variant	NM_001142503.3(STARD8):c.851C>T (p.Ala284Val)	not specified [RCV004865954]	uncertain significance	X	68717765	68717765	Human		name
597682811	CV3618424	single nucleotide variant	NM_001142503.3(STARD8):c.977G>A (p.Arg326His)	not specified [RCV004857684]	uncertain significance	X	68717891	68717891	Human		name
597682849	CV3618430	single nucleotide variant	NM_001142503.3(STARD8):c.991C>A (p.Gln331Lys)	not specified [RCV004857688]	uncertain significance	X	68717905	68717905	Human		name
597682880	CV3618434	single nucleotide variant	NM_001142503.3(STARD8):c.355C>A (p.Gln119Lys)	not specified [RCV004857691]	uncertain significance	X	68717269	68717269	Human		name
15170830	CV729684	single nucleotide variant	NM_001142503.3(STARD8):c.739A>G (p.Ser247Gly)	not provided [RCV000883542]\|not specified [RCV004028326]	likely benign\|uncertain significance	X	68717653	68717653	Human		name
155795933	CV1859366	single nucleotide variant	NM_001142503.3(STARD8):c.2978G>A (p.Ser993Asn)	not provided [RCV002464995]	uncertain significance	X	68723804	68723804	Human		name
156400416	CV2199170	single nucleotide variant	NM_001142503.3(STARD8):c.1183G>A (p.Val395Met)	not specified [RCV004080560]	uncertain significance	X	68718097	68718097	Human		name
156179687	CV2201678	single nucleotide variant	NM_001142503.3(STARD8):c.2632C>T (p.Pro878Ser)	not specified [RCV004082133]	uncertain significance	X	68722479	68722479	Human		name
155981466	CV2212292	single nucleotide variant	NM_001142503.3(STARD8):c.2740C>T (p.Arg914Cys)	not specified [RCV004090952]	uncertain significance	X	68722587	68722587	Human		name
156115820	CV2221566	single nucleotide variant	NM_001142503.3(STARD8):c.2438A>G (p.Lys813Arg)	not specified [RCV004096829]	uncertain significance	X	68721725	68721725	Human		name
156255448	CV2229296	single nucleotide variant	NM_001142503.3(STARD8):c.2617G>T (p.Ala873Ser)	not specified [RCV004101096]	uncertain significance	X	68722464	68722464	Human		name
156284999	CV2317597	single nucleotide variant	NM_001142503.3(STARD8):c.2254C>T (p.Pro752Ser)	not specified [RCV004172542]	uncertain significance	X	68721541	68721541	Human		name
155938505	CV2380777	single nucleotide variant	NM_001142503.3(STARD8):c.1454C>G (p.Pro485Arg)	not specified [RCV004218341]	uncertain significance	X	68718368	68718368	Human		name
329384143	CV2434973	single nucleotide variant	NM_001142503.3(STARD8):c.1217C>A (p.Ser406Tyr)	not specified [RCV004250840]	uncertain significance	X	68718131	68718131	Human		name
329352271	CV2452281	single nucleotide variant	NM_001142503.3(STARD8):c.2732C>A (p.Ala911Asp)	not specified [RCV004278964]	uncertain significance	X	68722579	68722579	Human		name
329390580	CV2455315	single nucleotide variant	NM_001142503.3(STARD8):c.1220G>C (p.Arg407Pro)	not specified [RCV004274823]	uncertain significance	X	68718134	68718134	Human		name
401743016	CV2694034	single nucleotide variant	NM_001142503.3(STARD8):c.1444G>A (p.Ala482Thr)	not specified [RCV004302474]	likely benign	X	68718358	68718358	Human		name
401758969	CV2694368	single nucleotide variant	NM_001142503.3(STARD8):c.1934G>A (p.Arg645Gln)	not specified [RCV004304558]	uncertain significance	X	68720308	68720308	Human		name
401783104	CV2703788	single nucleotide variant	NM_001142503.3(STARD8):c.1025G>A (p.Arg342Gln)	not specified [RCV004306660]	uncertain significance	X	68717939	68717939	Human		name
401723709	CV2725003	single nucleotide variant	NM_001142503.3(STARD8):c.1021C>T (p.Arg341Cys)	not specified [RCV004319762]	uncertain significance	X	68717935	68717935	Human		name
401777542	CV2728969	single nucleotide variant	NM_001142503.3(STARD8):c.1454C>T (p.Pro485Leu)	not specified [RCV004331691]	uncertain significance	X	68718368	68718368	Human		name
401855539	CV2757389	single nucleotide variant	NM_001142503.3(STARD8):c.2884C>T (p.Arg962Trp)	not specified [RCV004340789]	uncertain significance	X	68723710	68723710	Human		name
401860095	CV2765468	single nucleotide variant	NM_001142503.3(STARD8):c.2894C>A (p.Ala965Asp)	not specified [RCV004341781]	uncertain significance	X	68723720	68723720	Human		name
401873572	CV2776618	single nucleotide variant	NM_001142503.3(STARD8):c.1948T>C (p.Phe650Leu)	not specified [RCV004357493]	uncertain significance	X	68720322	68720322	Human		name
401927241	CV2829181	single nucleotide variant	NM_001142503.3(STARD8):c.1403C>A (p.Ala468Asp)	not provided [RCV003438461]	uncertain significance	X	68718317	68718317	Human		name
401927243	CV2829183	single nucleotide variant	NM_001142503.3(STARD8):c.1472C>T (p.Pro491Leu)	not provided [RCV003438463]	likely benign	X	68718386	68718386	Human		name
401927246	CV2829185	single nucleotide variant	NM_001142503.3(STARD8):c.2429A>G (p.Asn810Ser)	not provided [RCV003438465]\|not specified [RCV004364650]	likely benign\|uncertain significance	X	68721716	68721716	Human		name
405723053	CV3323791	single nucleotide variant	NM_001142503.3(STARD8):c.1061C>T (p.Thr354Met)	not specified [RCV004463393]	uncertain significance	X	68717975	68717975	Human		name
405723063	CV3323792	single nucleotide variant	NM_001142503.3(STARD8):c.1154A>G (p.Tyr385Cys)	not specified [RCV004463394]	uncertain significance	X	68718068	68718068	Human		name
405738751	CV3323793	single nucleotide variant	NM_001142503.3(STARD8):c.1168G>A (p.Asp390Asn)	not specified [RCV004465378]	uncertain significance	X	68718082	68718082	Human		name
405738758	CV3323794	single nucleotide variant	NM_001142503.3(STARD8):c.1318G>T (p.Ala440Ser)	not specified [RCV004465379]	uncertain significance	X	68718232	68718232	Human		name
405738766	CV3323795	single nucleotide variant	NM_001142503.3(STARD8):c.1597A>C (p.Ser533Arg)	not specified [RCV004465380]	uncertain significance	X	68718511	68718511	Human		name
405738776	CV3323796	single nucleotide variant	NM_001142503.3(STARD8):c.1676G>A (p.Arg559His)	not specified [RCV004465381]	uncertain significance	X	68718590	68718590	Human		name
405738782	CV3323797	single nucleotide variant	NM_001142503.3(STARD8):c.1747C>T (p.His583Tyr)	not specified [RCV004465382]	uncertain significance	X	68719256	68719256	Human		name
405738788	CV3323798	single nucleotide variant	NM_001142503.3(STARD8):c.1786C>T (p.Arg596Trp)	not specified [RCV004465383]	uncertain significance	X	68719295	68719295	Human		name
405738799	CV3323799	single nucleotide variant	NM_001142503.3(STARD8):c.2112G>T (p.Glu704Asp)	not specified [RCV004465384]	uncertain significance	X	68720986	68720986	Human		name
405738807	CV3323800	single nucleotide variant	NM_001142503.3(STARD8):c.2125A>G (p.Asn709Asp)	not specified [RCV004465385]	uncertain significance	X	68720999	68720999	Human		name
405738813	CV3323801	single nucleotide variant	NM_001142503.3(STARD8):c.2272G>A (p.Ala758Thr)	not specified [RCV004465386]	uncertain significance	X	68721559	68721559	Human		name
405738822	CV3323802	single nucleotide variant	NM_001142503.3(STARD8):c.2552G>A (p.Ser851Asn)	not specified [RCV004465387]	uncertain significance	X	68722139	68722139	Human		name
405738829	CV3323803	single nucleotide variant	NM_001142503.3(STARD8):c.2678G>C (p.Gly893Ala)	not specified [RCV004465388]	uncertain significance	X	68722525	68722525	Human		name
405738833	CV3323804	single nucleotide variant	NM_001142503.3(STARD8):c.2725C>G (p.Arg909Gly)	not specified [RCV004465389]	uncertain significance	X	68722572	68722572	Human		name
407495826	CV3485323	single nucleotide variant	NM_001142503.3(STARD8):c.2483T>C (p.Ile828Thr)	not specified [RCV004667971]	uncertain significance	X	68722070	68722070	Human		name
407495836	CV3485325	single nucleotide variant	NM_001142503.3(STARD8):c.2815C>G (p.Pro939Ala)	not specified [RCV004667973]	uncertain significance	X	68723641	68723641	Human		name
407495842	CV3485326	single nucleotide variant	NM_001142503.3(STARD8):c.1724G>A (p.Arg575His)	not specified [RCV004667974]	uncertain significance	X	68719233	68719233	Human		name
407495846	CV3485327	single nucleotide variant	NM_001142503.3(STARD8):c.1675C>T (p.Arg559Cys)	not specified [RCV004667975]	uncertain significance	X	68718589	68718589	Human		name
407495868	CV3485332	single nucleotide variant	NM_001142503.3(STARD8):c.1466C>T (p.Pro489Leu)	not specified [RCV004667980]	uncertain significance	X	68718380	68718380	Human		name
407495873	CV3485333	single nucleotide variant	NM_001142503.3(STARD8):c.1043C>T (p.Thr348Met)	not specified [RCV004667981]	uncertain significance	X	68717957	68717957	Human		name
597746840	CV3618419	single nucleotide variant	NM_001142503.3(STARD8):c.2780C>T (p.Thr927Met)	not specified [RCV004865952]	uncertain significance	X	68722627	68722627	Human		name
597682802	CV3618422	single nucleotide variant	NM_001142503.3(STARD8):c.1667G>A (p.Arg556His)	not specified [RCV004857683]	uncertain significance	X	68718581	68718581	Human		name
597746855	CV3618423	single nucleotide variant	NM_001142503.3(STARD8):c.1448A>G (p.Glu483Gly)	not specified [RCV004865955]	uncertain significance	X	68718362	68718362	Human		name
597682819	CV3618425	single nucleotide variant	NM_001142503.3(STARD8):c.1672C>T (p.Arg558Trp)	not specified [RCV004857685]	uncertain significance	X	68718586	68718586	Human		name
597746859	CV3618427	single nucleotide variant	NM_001142503.3(STARD8):c.1346A>G (p.His449Arg)	not specified [RCV004865956]	uncertain significance	X	68718260	68718260	Human		name
597682840	CV3618428	single nucleotide variant	NM_001142503.3(STARD8):c.2285C>T (p.Ala762Val)	not specified [RCV004857687]	uncertain significance	X	68721572	68721572	Human		name
597746865	CV3618431	single nucleotide variant	NM_001142503.3(STARD8):c.1720C>T (p.Leu574Phe)	not specified [RCV004865957]	uncertain significance	X	68719229	68719229	Human		name
597746870	CV3618435	single nucleotide variant	NM_001142503.3(STARD8):c.2296C>A (p.Leu766Met)	not specified [RCV004865958]	uncertain significance	X	68721583	68721583	Human		name
597746876	CV3618436	single nucleotide variant	NM_001142503.3(STARD8):c.1538T>C (p.Leu513Pro)	not specified [RCV004865959]	uncertain significance	X	68718452	68718452	Human		name
598250582	CV3919433	single nucleotide variant	NM_001142503.3(STARD8):c.1340C>T (p.Pro447Leu)	not specified [RCV005277736]	likely benign	X	68718254	68718254	Human		name
598250598	CV3919435	single nucleotide variant	NM_001142503.3(STARD8):c.2287G>A (p.Ala763Thr)	not specified [RCV005277738]	uncertain significance	X	68721574	68721574	Human		name
598213864	CV3919437	single nucleotide variant	NM_001142503.3(STARD8):c.2029C>T (p.Arg677Cys)	not specified [RCV005271093]	uncertain significance	X	68720403	68720403	Human		name
598250612	CV3919438	single nucleotide variant	NM_001142503.3(STARD8):c.2566C>T (p.Leu856Phe)	not specified [RCV005277740]	uncertain significance	X	68722153	68722153	Human		name
598250619	CV3919439	single nucleotide variant	NM_001142503.3(STARD8):c.2435C>T (p.Ser812Phe)	not specified [RCV005277741]	uncertain significance	X	68721722	68721722	Human		name
598250628	CV3919440	single nucleotide variant	NM_001142503.3(STARD8):c.1366G>C (p.Ala456Pro)	not specified [RCV005277742]	uncertain significance	X	68718280	68718280	Human		name
598250992	CV3919441	single nucleotide variant	NM_001142503.3(STARD8):c.2414C>T (p.Ser805Phe)	not specified [RCV005277743]	uncertain significance	X	68721701	68721701	Human		name
598250984	CV3919442	single nucleotide variant	NM_001142503.3(STARD8):c.1585A>G (p.Ser529Gly)	not specified [RCV005277744]	uncertain significance	X	68718499	68718499	Human		name
15203273	CV706291	single nucleotide variant	NM_001142503.3(STARD8):c.1284A>C (p.Glu428Asp)	not provided [RCV000958322]	benign	X	68718198	68718198	Human		name
15189091	CV774173	single nucleotide variant	NM_001142503.3(STARD8):c.1978C>T (p.Arg660Cys)	not provided [RCV000932138]	likely benign	X	68720352	68720352	Human		name
156283160	CV2334645	single nucleotide variant	NM_001142503.3(STARD8):c.3098C>T (p.Ser1033Leu)	not specified [RCV004188630]	uncertain significance	X	68724025	68724025	Human		name
156269416	CV2398576	single nucleotide variant	NM_001142503.3(STARD8):c.3058G>A (p.Val1020Ile)	not specified [RCV004237889]	uncertain significance	X	68723985	68723985	Human		name
401760643	CV2706030	single nucleotide variant	NM_001142503.3(STARD8):c.3139G>A (p.Glu1047Lys)	not specified [RCV004314731]	uncertain significance	X	68724066	68724066	Human		name
407495855	CV3485329	single nucleotide variant	NM_001142503.3(STARD8):c.3041G>A (p.Arg1014His)	not specified [RCV004667977]	uncertain significance	X	68723968	68723968	Human		name
597682870	CV3618433	single nucleotide variant	NM_001142503.3(STARD8):c.3026G>T (p.Arg1009Leu)	not specified [RCV004857690]	uncertain significance	X	68723953	68723953	Human		name
598250605	CV3919436	single nucleotide variant	NM_001142503.3(STARD8):c.3145T>C (p.Cys1049Arg)	not specified [RCV005277739]	uncertain significance	X	68724072	68724072	Human		name
401927242	CV2829182	deletion	NM_001142503.3(STARD8):c.1466_1483del (p.485PA[2])	not provided [RCV003438462]	likely benign	X	68718363	68718380	Human		name

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