Sec24c Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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105 records found for search term Sec24c

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15110226	CV730708	single nucleotide variant	NM_198597.3(SEC24C):c.1800-7T>C	not provided [RCV000894019]	benign	10	73766753	73766753	Human		name
15191149	CV730709	single nucleotide variant	NM_198597.3(SEC24C):c.3145-4G>A	not provided [RCV000888299]	benign	10	73770951	73770951	Human		name
15125937	CV779643	single nucleotide variant	NM_198597.3(SEC24C):c.850+10T>G	not provided [RCV000963662]	benign	10	73760396	73760396	Human		name
401899179	CV2783731	single nucleotide variant	NM_198597.3(SEC24C):c.40G>C (p.Gly14Arg)	not specified [RCV004360650]	uncertain significance	10	73746872	73746872	Human		name
597716685	CV3605559	single nucleotide variant	NM_198597.3(SEC24C):c.38T>C (p.Phe13Ser)	not specified [RCV004861587]	uncertain significance	10	73746870	73746870	Human		name
15177737	CV701429	single nucleotide variant	NM_198597.3(SEC24C):c.771C>G (p.Gly257=)	not provided [RCV000951110]	benign	10	73760307	73760307	Human		name
150337411	CV1165954	single nucleotide variant	NM_198597.3(SEC24C):c.2610G>A (p.Thr870=)	not provided [RCV001532606]	likely benign	10	73769661	73769661	Human		name
156116142	CV2273502	single nucleotide variant	NM_198597.3(SEC24C):c.284C>G (p.Pro95Arg)	not specified [RCV004132246]	uncertain significance	10	73751219	73751219	Human		name
405705229	CV3310772	single nucleotide variant	NM_198597.3(SEC24C):c.131A>G (p.Tyr44Cys)	not specified [RCV004447660]	uncertain significance	10	73746963	73746963	Human		name
405705340	CV3310785	single nucleotide variant	NM_198597.3(SEC24C):c.292A>G (p.Thr98Ala)	not specified [RCV004447673]	uncertain significance	10	73751227	73751227	Human		name
407425937	CV3409685	single nucleotide variant	NM_198597.3(SEC24C):c.2769C>G (p.Val923=)	not provided [RCV004585617]	likely benign	10	73769922	73769922	Human		name
407477144	CV3476724	single nucleotide variant	NM_198597.3(SEC24C):c.184G>A (p.Ala62Thr)	not specified [RCV004663649]	uncertain significance	10	73751119	73751119	Human		name
407477153	CV3476726	single nucleotide variant	NM_198597.3(SEC24C):c.128C>T (p.Ala43Val)	not specified [RCV004663651]	uncertain significance	10	73746960	73746960	Human		name
597716563	CV3605544	single nucleotide variant	NM_198597.3(SEC24C):c.164C>T (p.Pro55Leu)	not specified [RCV004861572]	uncertain significance	10	73746996	73746996	Human		name
597716617	CV3605551	single nucleotide variant	NM_198597.3(SEC24C):c.293C>G (p.Thr98Ser)	not specified [RCV004861579]	uncertain significance	10	73751228	73751228	Human		name
616937803	CV3732964	deletion	NM_198597.3(SEC24C):c.333del (p.Ser112fs)	Developmental and epileptic encephalopathy [RCV005412716]	likely pathogenic	10	73759644	73759644	Human	1	name
598211203	CV3907232	single nucleotide variant	NM_198597.3(SEC24C):c.271G>C (p.Val91Leu)	not specified [RCV005270783]	uncertain significance	10	73751206	73751206	Human		name
15187578	CV701430	single nucleotide variant	NM_198597.3(SEC24C):c.1698C>T (p.Ala566=)	not provided [RCV000953631]	benign	10	73766440	73766440	Human		name
15105402	CV712467	single nucleotide variant	NM_198597.3(SEC24C):c.2988C>T (p.Ser996=)	not provided [RCV000959878]	likely benign	10	73770405	73770405	Human		name
15169726	CV752261	single nucleotide variant	NM_198597.3(SEC24C):c.2874C>T (p.Pro958=)	not provided [RCV000927557]	likely benign	10	73770291	73770291	Human		name
8626852	CV81996	single nucleotide variant	NM_004922.3(SEC24C):c.1143C>T (p.Ile381=)	Malignant melanoma [RCV000062075]	not provided	10	73763899	73763899	Human		name
156027040	CV2242409	single nucleotide variant	NM_198597.3(SEC24C):c.872G>T (p.Gly291Val)	not specified [RCV004111409]	uncertain significance	10	73760734	73760734	Human		name
155916627	CV2336178	single nucleotide variant	NM_198597.3(SEC24C):c.526T>A (p.Ser176Thr)	not specified [RCV004189770]	uncertain significance	10	73760062	73760062	Human		name
155918960	CV2360113	single nucleotide variant	NM_198597.3(SEC24C):c.542C>G (p.Ser181Cys)	not specified [RCV004215388]	uncertain significance	10	73760078	73760078	Human		name
156383936	CV2361754	single nucleotide variant	NM_198597.3(SEC24C):c.439G>A (p.Gly147Ser)	not provided [RCV005425089]\|not specified [RCV004223229]	likely benign\|uncertain significance	10	73759752	73759752	Human		name
156247019	CV2396857	single nucleotide variant	NM_198597.3(SEC24C):c.317G>A (p.Gly106Glu)	not specified [RCV004233985]	uncertain significance	10	73759630	73759630	Human		name
329359292	CV2435384	single nucleotide variant	NM_198597.3(SEC24C):c.941A>C (p.Gln314Pro)	not specified [RCV004253039]	uncertain significance	10	73760803	73760803	Human		name
401740439	CV2681415	single nucleotide variant	NM_198597.3(SEC24C):c.463T>C (p.Ser155Pro)	not specified [RCV004291960]	likely benign	10	73759776	73759776	Human		name
401881724	CV2783935	single nucleotide variant	NM_198597.3(SEC24C):c.430C>G (p.Gln144Glu)	not specified [RCV004362357]	uncertain significance	10	73759743	73759743	Human		name
405705385	CV3310790	single nucleotide variant	NM_198597.3(SEC24C):c.422C>A (p.Ser141Tyr)	not specified [RCV004447678]	uncertain significance	10	73759735	73759735	Human		name
405705393	CV3310791	single nucleotide variant	NM_198597.3(SEC24C):c.491C>T (p.Thr164Ile)	not specified [RCV004447679]	uncertain significance	10	73760027	73760027	Human		name
405705402	CV3310792	single nucleotide variant	NM_198597.3(SEC24C):c.611G>A (p.Arg204Gln)	not specified [RCV004447680]	uncertain significance	10	73760147	73760147	Human		name
407477176	CV3476732	single nucleotide variant	NM_198597.3(SEC24C):c.986C>T (p.Pro329Leu)	not specified [RCV004663656]	uncertain significance	10	73760848	73760848	Human		name
597716572	CV3605545	single nucleotide variant	NM_198597.3(SEC24C):c.859G>A (p.Gly287Arg)	not specified [RCV004861573]	uncertain significance	10	73760721	73760721	Human		name
597716579	CV3605546	single nucleotide variant	NM_198597.3(SEC24C):c.748C>A (p.Pro250Thr)	not specified [RCV004861574]	uncertain significance	10	73760284	73760284	Human		name
597716586	CV3605547	single nucleotide variant	NM_198597.3(SEC24C):c.868C>T (p.Arg290Trp)	not specified [RCV004861575]	uncertain significance	10	73760730	73760730	Human		name
597716608	CV3605550	single nucleotide variant	NM_198597.3(SEC24C):c.664C>T (p.Arg222Trp)	not specified [RCV004861578]	uncertain significance	10	73760200	73760200	Human		name
597716638	CV3605553	single nucleotide variant	NM_198597.3(SEC24C):c.971A>G (p.Asp324Gly)	not specified [RCV004861581]	uncertain significance	10	73760833	73760833	Human		name
597716643	CV3605554	single nucleotide variant	NM_198597.3(SEC24C):c.623C>T (p.Ser208Leu)	not specified [RCV004861582]	uncertain significance	10	73760159	73760159	Human		name
597716654	CV3605555	single nucleotide variant	NM_198597.3(SEC24C):c.370C>T (p.Leu124Phe)	not specified [RCV004861583]	uncertain significance	10	73759683	73759683	Human		name
597716661	CV3605556	single nucleotide variant	NM_198597.3(SEC24C):c.304C>G (p.Gln102Glu)	not specified [RCV004861584]	uncertain significance	10	73751239	73751239	Human		name
598211116	CV3907217	single nucleotide variant	NM_198597.3(SEC24C):c.320C>T (p.Ser107Phe)	not specified [RCV005270768]	uncertain significance	10	73759633	73759633	Human		name
598211128	CV3907219	single nucleotide variant	NM_198597.3(SEC24C):c.641C>T (p.Thr214Ile)	not specified [RCV005270770]	uncertain significance	10	73760177	73760177	Human		name
598211143	CV3907222	single nucleotide variant	NM_198597.3(SEC24C):c.923G>A (p.Ser308Asn)	not specified [RCV005270773]	uncertain significance	10	73760785	73760785	Human		name
598211155	CV3907224	single nucleotide variant	NM_198597.3(SEC24C):c.725G>C (p.Ser242Thr)	not specified [RCV005270775]	uncertain significance	10	73760261	73760261	Human		name
598211162	CV3907225	single nucleotide variant	NM_198597.3(SEC24C):c.704G>A (p.Ser235Asn)	not specified [RCV005270776]	uncertain significance	10	73760240	73760240	Human		name
598211180	CV3907228	single nucleotide variant	NM_198597.3(SEC24C):c.832T>C (p.Tyr278His)	not specified [RCV005270779]	uncertain significance	10	73760368	73760368	Human		name
15202399	CV724063	single nucleotide variant	NM_198597.3(SEC24C):c.763C>G (p.Pro255Ala)	not provided [RCV000891462]	benign	10	73760299	73760299	Human		name
156185352	CV2195556	single nucleotide variant	NM_198597.3(SEC24C):c.1637G>A (p.Arg546His)	not specified [RCV004082770]	uncertain significance	10	73766379	73766379	Human		name
155928967	CV2224472	single nucleotide variant	NM_198597.3(SEC24C):c.1529T>C (p.Val510Ala)	not specified [RCV004098067]	uncertain significance	10	73766132	73766132	Human		name
156178517	CV2258248	single nucleotide variant	NM_198597.3(SEC24C):c.1655A>G (p.Tyr552Cys)	not specified [RCV004121619]	uncertain significance	10	73766397	73766397	Human		name
156089510	CV2259129	single nucleotide variant	NM_198597.3(SEC24C):c.2398A>G (p.Asn800Asp)	not specified [RCV004120380]	uncertain significance	10	73769126	73769126	Human		name
156055409	CV2269644	single nucleotide variant	NM_198597.3(SEC24C):c.2602C>A (p.Arg868Ser)	not specified [RCV004126645]	uncertain significance	10	73769653	73769653	Human		name
155923838	CV2280396	single nucleotide variant	NM_198597.3(SEC24C):c.2379C>A (p.Phe793Leu)	not specified [RCV004140578]	uncertain significance	10	73769107	73769107	Human		name
156089898	CV2295624	single nucleotide variant	NM_198597.3(SEC24C):c.2257A>G (p.Met753Val)	not specified [RCV004160707]	uncertain significance	10	73768885	73768885	Human		name
156155153	CV2359698	single nucleotide variant	NM_198597.3(SEC24C):c.1327A>G (p.Arg443Gly)	not specified [RCV004210521]	uncertain significance	10	73765550	73765550	Human		name
156339950	CV2367762	single nucleotide variant	NM_198597.3(SEC24C):c.1486A>G (p.Asn496Asp)	not specified [RCV004213717]	uncertain significance	10	73766089	73766089	Human		name
156040038	CV2384323	single nucleotide variant	NM_198597.3(SEC24C):c.2219G>A (p.Arg740His)	not specified [RCV004227705]	uncertain significance	10	73768847	73768847	Human		name
329368122	CV2424190	single nucleotide variant	NM_198597.3(SEC24C):c.1330C>T (p.Arg444Cys)	not specified [RCV004250317]	uncertain significance	10	73765553	73765553	Human		name
401771600	CV2686251	single nucleotide variant	NM_198597.3(SEC24C):c.2494T>G (p.Cys832Gly)	not specified [RCV004297337]	uncertain significance	10	73769416	73769416	Human		name
401725203	CV2697311	single nucleotide variant	NM_198597.3(SEC24C):c.2201G>A (p.Arg734Gln)	not specified [RCV004304069]	uncertain significance	10	73768829	73768829	Human		name
401781596	CV2722179	single nucleotide variant	NM_198597.3(SEC24C):c.2494T>C (p.Cys832Arg)	not specified [RCV004328748]	uncertain significance	10	73769416	73769416	Human		name
401860664	CV2758564	single nucleotide variant	NM_198597.3(SEC24C):c.2587C>T (p.Pro863Ser)	not specified [RCV004337652]	uncertain significance	10	73769638	73769638	Human		name
401862474	CV2775320	single nucleotide variant	NM_198597.3(SEC24C):c.1960A>G (p.Lys654Glu)	not specified [RCV004348432]	uncertain significance	10	73767120	73767120	Human		name
401876410	CV2785885	single nucleotide variant	NM_198597.3(SEC24C):c.2393G>A (p.Arg798Gln)	not specified [RCV004365406]	uncertain significance	10	73769121	73769121	Human		name
405705242	CV3310773	single nucleotide variant	NM_198597.3(SEC24C):c.1321G>A (p.Gly441Arg)	not specified [RCV004447661]	uncertain significance	10	73765544	73765544	Human		name
405705251	CV3310774	single nucleotide variant	NM_198597.3(SEC24C):c.1469T>C (p.Val490Ala)	not specified [RCV004447662]	uncertain significance	10	73765902	73765902	Human		name
405705258	CV3310775	single nucleotide variant	NM_198597.3(SEC24C):c.1563G>C (p.Arg521Ser)	not specified [RCV004447663]	uncertain significance	10	73766166	73766166	Human		name
405705265	CV3310776	single nucleotide variant	NM_198597.3(SEC24C):c.1616G>A (p.Gly539Glu)	not specified [RCV004447664]	uncertain significance	10	73766358	73766358	Human		name
405705283	CV3310778	single nucleotide variant	NM_198597.3(SEC24C):c.1771G>A (p.Val591Ile)	not specified [RCV004447666]	uncertain significance	10	73766513	73766513	Human		name
405705291	CV3310779	single nucleotide variant	NM_198597.3(SEC24C):c.2191G>A (p.Asp731Asn)	not specified [RCV004447667]	uncertain significance	10	73768819	73768819	Human		name
405705298	CV3310780	single nucleotide variant	NM_198597.3(SEC24C):c.2392C>T (p.Arg798Trp)	not specified [RCV004447668]	uncertain significance	10	73769120	73769120	Human		name
405705309	CV3310781	single nucleotide variant	NM_198597.3(SEC24C):c.2602C>T (p.Arg868Cys)	not specified [RCV004447669]	uncertain significance	10	73769653	73769653	Human		name
405705317	CV3310782	single nucleotide variant	NM_198597.3(SEC24C):c.2614A>T (p.Ile872Phe)	not specified [RCV004447670]	uncertain significance	10	73769665	73769665	Human		name
405705327	CV3310783	single nucleotide variant	NM_198597.3(SEC24C):c.2836T>G (p.Phe946Val)	not specified [RCV004447671]	uncertain significance	10	73769989	73769989	Human		name
405705350	CV3310786	single nucleotide variant	NM_198597.3(SEC24C):c.2930A>T (p.Asn977Ile)	not specified [RCV004447674]	uncertain significance	10	73770347	73770347	Human		name
407477140	CV3476723	single nucleotide variant	NM_198597.3(SEC24C):c.2371G>T (p.Val791Leu)	not specified [RCV004663648]	uncertain significance	10	73769099	73769099	Human		name
407477148	CV3476725	single nucleotide variant	NM_198597.3(SEC24C):c.2994A>C (p.Gln998His)	not specified [RCV004663650]	uncertain significance	10	73770411	73770411	Human		name
407477157	CV3476727	single nucleotide variant	NM_198597.3(SEC24C):c.2126T>A (p.Leu709His)	not specified [RCV004663652]	uncertain significance	10	73767952	73767952	Human		name
407477161	CV3476728	single nucleotide variant	NM_198597.3(SEC24C):c.2602C>G (p.Arg868Gly)	not specified [RCV004663653]	uncertain significance	10	73769653	73769653	Human		name
407477166	CV3476729	single nucleotide variant	NM_198597.3(SEC24C):c.2281A>G (p.Ile761Val)	not specified [RCV004663654]	uncertain significance	10	73769009	73769009	Human		name
407477171	CV3476730	single nucleotide variant	NM_198597.3(SEC24C):c.2385T>G (p.His795Gln)	not specified [RCV004663655]	uncertain significance	10	73769113	73769113	Human		name
407492116	CV3476731	single nucleotide variant	NM_198597.3(SEC24C):c.1024A>G (p.Thr342Ala)	not specified [RCV004667030]	uncertain significance	10	73763526	73763526	Human		name
407477183	CV3476734	single nucleotide variant	NM_198597.3(SEC24C):c.2930A>G (p.Asn977Ser)	not specified [RCV004663658]	uncertain significance	10	73770347	73770347	Human		name
597716593	CV3605548	single nucleotide variant	NM_198597.3(SEC24C):c.2440A>T (p.Thr814Ser)	not specified [RCV004861576]	uncertain significance	10	73769362	73769362	Human		name
597716602	CV3605549	single nucleotide variant	NM_198597.3(SEC24C):c.1928A>G (p.His643Arg)	not specified [RCV004861577]	uncertain significance	10	73767088	73767088	Human		name
597716626	CV3605552	single nucleotide variant	NM_198597.3(SEC24C):c.2447G>C (p.Cys816Ser)	not specified [RCV004861580]	uncertain significance	10	73769369	73769369	Human		name
597716668	CV3605557	single nucleotide variant	NM_198597.3(SEC24C):c.1550C>T (p.Thr517Ile)	not specified [RCV004861585]	uncertain significance	10	73766153	73766153	Human		name
597716676	CV3605558	single nucleotide variant	NM_198597.3(SEC24C):c.2410G>A (p.Gly804Arg)	not specified [RCV004861586]	uncertain significance	10	73769138	73769138	Human		name
598211122	CV3907218	single nucleotide variant	NM_198597.3(SEC24C):c.1982G>A (p.Arg661Lys)	not specified [RCV005270769]	uncertain significance	10	73767142	73767142	Human		name
598211137	CV3907221	single nucleotide variant	NM_198597.3(SEC24C):c.1636C>T (p.Arg546Cys)	not specified [RCV005270772]	uncertain significance	10	73766378	73766378	Human		name
598211148	CV3907223	single nucleotide variant	NM_198597.3(SEC24C):c.1223A>T (p.Glu408Val)	not specified [RCV005270774]	uncertain significance	10	73763979	73763979	Human		name
598211168	CV3907226	single nucleotide variant	NM_198597.3(SEC24C):c.2119G>A (p.Ala707Thr)	not specified [RCV005270777]	uncertain significance	10	73767945	73767945	Human		name
598211174	CV3907227	single nucleotide variant	NM_198597.3(SEC24C):c.2921G>A (p.Arg974His)	not specified [RCV005270778]	uncertain significance	10	73770338	73770338	Human		name
598211184	CV3907229	single nucleotide variant	NM_198597.3(SEC24C):c.2662A>G (p.Ser888Gly)	not specified [RCV005270780]	uncertain significance	10	73769713	73769713	Human		name
598211192	CV3907230	single nucleotide variant	NM_198597.3(SEC24C):c.2567A>G (p.Tyr856Cys)	not specified [RCV005270781]	uncertain significance	10	73769618	73769618	Human		name
598211197	CV3907231	single nucleotide variant	NM_198597.3(SEC24C):c.1108A>G (p.Ser370Gly)	not specified [RCV005270782]	uncertain significance	10	73763864	73763864	Human		name
38597102	CV801868	single nucleotide variant	NM_198597.3(SEC24C):c.1500C>A (p.Ser500Arg)	Microcephaly [RCV001252937]	uncertain significance	10	73766103	73766103	Human	2	name
8626851	CV81995	single nucleotide variant	NM_004922.3(SEC24C):c.1030C>T (p.Pro344Ser)	Malignant melanoma [RCV000062074]	not provided	10	73763532	73763532	Human		name
155919438	CV2279418	single nucleotide variant	NM_198597.3(SEC24C):c.3168C>G (p.Asp1056Glu)	not specified [RCV004141960]	uncertain significance	10	73770978	73770978	Human		name
156182407	CV2298612	single nucleotide variant	NM_198597.3(SEC24C):c.3220G>T (p.Gly1074Trp)	not specified [RCV004162259]	uncertain significance	10	73771030	73771030	Human		name
329400354	CV2441560	single nucleotide variant	NM_198597.3(SEC24C):c.3154G>T (p.Val1052Leu)	not specified [RCV004257344]	uncertain significance	10	73770964	73770964	Human		name
401883698	CV2785739	single nucleotide variant	NM_198597.3(SEC24C):c.3026C>G (p.Ser1009Cys)	not specified [RCV004364994]	uncertain significance	10	73770443	73770443	Human		name
405705357	CV3310787	single nucleotide variant	NM_198597.3(SEC24C):c.3068T>G (p.Val1023Gly)	not specified [RCV004447675]	uncertain significance	10	73770722	73770722	Human		name
405705369	CV3310788	single nucleotide variant	NM_198597.3(SEC24C):c.3196C>G (p.Leu1066Val)	not specified [RCV004447676]	uncertain significance	10	73771006	73771006	Human		name

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