Sec24a Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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85 records found for search term Sec24a

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156343888	CV2349288	single nucleotide variant	NM_021982.3(SEC24A):c.95A>G (p.Asn32Ser)	not specified [RCV004199235]	uncertain significance	5	134649171	134649171	Human		name
598210964	CV3907194	single nucleotide variant	NM_021982.3(SEC24A):c.62G>C (p.Gly21Ala)	not specified [RCV005270745]	uncertain significance	5	134649138	134649138	Human		name
156193278	CV2344222	single nucleotide variant	NM_021982.3(SEC24A):c.203A>G (p.Asn68Ser)	not specified [RCV004197859]	uncertain significance	5	134661224	134661224	Human		name
401883440	CV2785659	single nucleotide variant	NM_021982.3(SEC24A):c.278C>G (p.Ser93Cys)	not specified [RCV004363157]	uncertain significance	5	134661299	134661299	Human		name
405704974	CV3310738	single nucleotide variant	NM_021982.3(SEC24A):c.195G>T (p.Lys65Asn)	not specified [RCV004447626]	uncertain significance	5	134661216	134661216	Human		name
405704983	CV3310739	single nucleotide variant	NM_021982.3(SEC24A):c.256C>G (p.Leu86Val)	not specified [RCV004447627]	uncertain significance	5	134661277	134661277	Human		name
596946828	CV3548661	single nucleotide variant	NM_021982.3(SEC24A):c.1038G>A (p.Glu346=)	not provided [RCV004810489]	likely benign	5	134675104	134675104	Human		name
597716292	CV3605512	single nucleotide variant	NM_021982.3(SEC24A):c.113C>T (p.Ala38Val)	not specified [RCV004861543]	uncertain significance	5	134661134	134661134	Human		name
597716337	CV3605518	single nucleotide variant	NM_021982.3(SEC24A):c.242G>A (p.Gly81Glu)	not specified [RCV004861548]	uncertain significance	5	134661263	134661263	Human		name
598210944	CV3907191	single nucleotide variant	NM_021982.3(SEC24A):c.128A>G (p.Gln43Arg)	not specified [RCV005270742]	uncertain significance	5	134661149	134661149	Human		name
598210951	CV3907192	single nucleotide variant	NM_021982.3(SEC24A):c.1950A>G (p.Lys650=)	not specified [RCV005270743]	likely benign	5	134693897	134693897	Human		name
155924714	CV2211630	single nucleotide variant	NM_021982.3(SEC24A):c.658C>T (p.Pro220Ser)	not specified [RCV004084524]	uncertain significance	5	134666915	134666915	Human		name
155903293	CV2274853	single nucleotide variant	NM_021982.3(SEC24A):c.751A>G (p.Asn251Asp)	not specified [RCV004133051]	uncertain significance	5	134671820	134671820	Human		name
155920390	CV2279586	single nucleotide variant	NM_021982.3(SEC24A):c.416A>C (p.Gln139Pro)	not specified [RCV004142087]	uncertain significance	5	134661437	134661437	Human		name
156138954	CV2280711	single nucleotide variant	NM_021982.3(SEC24A):c.790G>A (p.Asp264Asn)	not specified [RCV004143169]	uncertain significance	5	134671859	134671859	Human		name
156237377	CV2285799	single nucleotide variant	NM_021982.3(SEC24A):c.503C>A (p.Thr168Asn)	not specified [RCV004143749]	uncertain significance	5	134661524	134661524	Human		name
156082601	CV2301179	single nucleotide variant	NM_021982.3(SEC24A):c.401C>A (p.Pro134Gln)	not specified [RCV004160087]	uncertain significance	5	134661422	134661422	Human		name
155981115	CV2343734	single nucleotide variant	NM_021982.3(SEC24A):c.854G>A (p.Ser285Asn)	not specified [RCV004190757]	uncertain significance	5	134674651	134674651	Human		name
156004854	CV2396999	single nucleotide variant	NM_021982.3(SEC24A):c.644C>T (p.Ala215Val)	not specified [RCV004236152]	uncertain significance	5	134666901	134666901	Human		name
156095892	CV2399011	single nucleotide variant	NM_021982.3(SEC24A):c.352A>C (p.Thr118Pro)	not specified [RCV004245315]	uncertain significance	5	134661373	134661373	Human		name
329401832	CV2457478	single nucleotide variant	NM_021982.3(SEC24A):c.470C>A (p.Ser157Tyr)	not specified [RCV004267296]	uncertain significance	5	134661491	134661491	Human		name
405705027	CV3310745	single nucleotide variant	NM_021982.3(SEC24A):c.322A>G (p.Met108Val)	not specified [RCV004447633]	uncertain significance	5	134661343	134661343	Human		name
405705041	CV3310747	single nucleotide variant	NM_021982.3(SEC24A):c.617C>T (p.Pro206Leu)	not specified [RCV004447635]	uncertain significance	5	134666874	134666874	Human		name
405705048	CV3310748	single nucleotide variant	NM_021982.3(SEC24A):c.622G>C (p.Ala208Pro)	not specified [RCV004447636]	uncertain significance	5	134666879	134666879	Human		name
407477080	CV3476702	single nucleotide variant	NM_021982.3(SEC24A):c.907A>C (p.Thr303Pro)	not specified [RCV004663634]	uncertain significance	5	134674704	134674704	Human		name
407492099	CV3476709	single nucleotide variant	NM_021982.3(SEC24A):c.698A>T (p.Asp233Val)	not specified [RCV004667026]	uncertain significance	5	134666955	134666955	Human		name
597716264	CV3605509	single nucleotide variant	NM_021982.3(SEC24A):c.358C>T (p.Pro120Ser)	not specified [RCV004861540]	uncertain significance	5	134661379	134661379	Human		name
597716317	CV3605516	single nucleotide variant	NM_021982.3(SEC24A):c.697G>A (p.Asp233Asn)	not specified [RCV004861546]	uncertain significance	5	134666954	134666954	Human		name
597716354	CV3605520	single nucleotide variant	NM_021982.3(SEC24A):c.443A>G (p.Gln148Arg)	not specified [RCV004861550]	uncertain significance	5	134661464	134661464	Human		name
598210877	CV3907182	single nucleotide variant	NM_021982.3(SEC24A):c.806G>A (p.Gly269Asp)	not specified [RCV005270733]	uncertain significance	5	134671875	134671875	Human		name
598210958	CV3907193	single nucleotide variant	NM_021982.3(SEC24A):c.298C>T (p.Leu100Phe)	not specified [RCV005270744]	uncertain significance	5	134661319	134661319	Human		name
8631377	CV86538	single nucleotide variant	NM_021982.2(SEC24A):c.335C>T (p.Ala112Val)	Malignant melanoma [RCV000066629]	not provided	5	134661356	134661356	Human		name
156374142	CV2198270	single nucleotide variant	NM_021982.3(SEC24A):c.1510C>A (p.Pro504Thr)	not provided [RCV004695347]\|not specified [RCV004081826]	uncertain significance	5	134686808	134686808	Human		name
156258265	CV2204646	single nucleotide variant	NM_021982.3(SEC24A):c.2756G>A (p.Arg919His)	not specified [RCV004081751]	uncertain significance	5	134715052	134715052	Human		name
156225501	CV2219611	single nucleotide variant	NM_021982.3(SEC24A):c.1692A>T (p.Gln564His)	not specified [RCV004095335]	uncertain significance	5	134688268	134688268	Human		name
156137728	CV2236494	single nucleotide variant	NM_021982.3(SEC24A):c.2158C>T (p.His720Tyr)	not specified [RCV004110496]	uncertain significance	5	134697949	134697949	Human		name
156037631	CV2239533	single nucleotide variant	NM_021982.3(SEC24A):c.2894T>C (p.Ile965Thr)	not specified [RCV004114533]	uncertain significance	5	134718097	134718097	Human		name
156088852	CV2241432	single nucleotide variant	NM_021982.3(SEC24A):c.1211A>C (p.Lys404Thr)	not specified [RCV004104345]	uncertain significance	5	134676082	134676082	Human		name
156112601	CV2267514	single nucleotide variant	NM_021982.3(SEC24A):c.2777C>T (p.Ala926Val)	not specified [RCV004135937]	uncertain significance	5	134715073	134715073	Human		name
156034525	CV2282901	single nucleotide variant	NM_021982.3(SEC24A):c.1657A>G (p.Ile553Val)	not specified [RCV004143544]	uncertain significance	5	134688233	134688233	Human		name
155992992	CV2286258	single nucleotide variant	NM_021982.3(SEC24A):c.2174C>T (p.Pro725Leu)	not specified [RCV004146217]	uncertain significance	5	134697965	134697965	Human		name
156198017	CV2306841	single nucleotide variant	NM_021982.3(SEC24A):c.2486C>T (p.Ser829Leu)	not specified [RCV004159408]	uncertain significance	5	134705372	134705372	Human		name
156038778	CV2332658	single nucleotide variant	NM_021982.3(SEC24A):c.2916G>T (p.Gln972His)	not specified [RCV004189335]	uncertain significance	5	134718119	134718119	Human		name
155926272	CV2345140	single nucleotide variant	NM_021982.3(SEC24A):c.2656C>G (p.Gln886Glu)	not specified [RCV004195882]	uncertain significance	5	134708817	134708817	Human		name
401772783	CV2687813	single nucleotide variant	NM_021982.3(SEC24A):c.2153C>G (p.Ser718Cys)	not specified [RCV004302793]	uncertain significance	5	134697944	134697944	Human		name
401877646	CV2761243	single nucleotide variant	NM_021982.3(SEC24A):c.1384C>T (p.Pro462Ser)	not specified [RCV004341120]	uncertain significance	5	134682375	134682375	Human		name
401875738	CV2789149	single nucleotide variant	NM_021982.3(SEC24A):c.1342A>T (p.Arg448Trp)	not specified [RCV004365199]	uncertain significance	5	134679689	134679689	Human		name
405704938	CV3310733	single nucleotide variant	NM_021982.3(SEC24A):c.1077G>A (p.Met359Ile)	not specified [RCV004447621]	uncertain significance	5	134675143	134675143	Human		name
405704946	CV3310734	single nucleotide variant	NM_021982.3(SEC24A):c.1082C>T (p.Pro361Leu)	not specified [RCV004447622]	uncertain significance	5	134675148	134675148	Human		name
405704951	CV3310735	single nucleotide variant	NM_021982.3(SEC24A):c.1166C>T (p.Thr389Met)	not specified [RCV004447623]	uncertain significance	5	134676037	134676037	Human		name
405704958	CV3310736	single nucleotide variant	NM_021982.3(SEC24A):c.1795C>G (p.Leu599Val)	not specified [RCV004447624]	uncertain significance	5	134693742	134693742	Human		name
405704968	CV3310737	single nucleotide variant	NM_021982.3(SEC24A):c.1945C>G (p.Leu649Val)	not specified [RCV004447625]	uncertain significance	5	134693892	134693892	Human		name
405704991	CV3310740	single nucleotide variant	NM_021982.3(SEC24A):c.2590C>G (p.Arg864Gly)	not specified [RCV004447628]	uncertain significance	5	134708751	134708751	Human		name
405704999	CV3310741	single nucleotide variant	NM_021982.3(SEC24A):c.2635C>T (p.Arg879Cys)	not specified [RCV004447629]	uncertain significance	5	134708796	134708796	Human		name
405705013	CV3310743	single nucleotide variant	NM_021982.3(SEC24A):c.2875A>G (p.Asn959Asp)	not specified [RCV004447631]	uncertain significance	5	134718078	134718078	Human		name
407477075	CV3476700	single nucleotide variant	NM_021982.3(SEC24A):c.2306G>A (p.Arg769Lys)	not specified [RCV004663633]	uncertain significance	5	134703798	134703798	Human		name
407492087	CV3476703	single nucleotide variant	NM_021982.3(SEC24A):c.2644G>A (p.Val882Ile)	not specified [RCV004667023]	uncertain significance	5	134708805	134708805	Human		name
407477086	CV3476704	single nucleotide variant	NM_021982.3(SEC24A):c.2945G>A (p.Gly982Glu)	not specified [RCV004663635]	uncertain significance	5	134718148	134718148	Human		name
407477093	CV3476706	single nucleotide variant	NM_021982.3(SEC24A):c.2350G>C (p.Gly784Arg)	not specified [RCV004663636]	uncertain significance	5	134703842	134703842	Human		name
407492095	CV3476707	single nucleotide variant	NM_021982.3(SEC24A):c.2636G>A (p.Arg879His)	not specified [RCV004667025]	uncertain significance	5	134708797	134708797	Human		name
407477101	CV3476710	single nucleotide variant	NM_021982.3(SEC24A):c.1324G>A (p.Val442Ile)	not specified [RCV004663638]	uncertain significance	5	134679671	134679671	Human		name
407477105	CV3476711	single nucleotide variant	NM_021982.3(SEC24A):c.2926G>C (p.Glu976Gln)	not specified [RCV004663639]	uncertain significance	5	134718129	134718129	Human		name
596941345	CV3542482	single nucleotide variant	NM_021982.3(SEC24A):c.2071C>T (p.Leu691Phe)	Progressive spinal muscular atrophy [RCV004797728]	uncertain significance	5	134697210	134697210	Human	2	name
597716231	CV3605506	single nucleotide variant	NM_021982.3(SEC24A):c.1211A>G (p.Lys404Arg)	not specified [RCV004861537]	uncertain significance	5	134676082	134676082	Human		name
597716242	CV3605507	single nucleotide variant	NM_021982.3(SEC24A):c.1595A>G (p.Asn532Ser)	not specified [RCV004861538]	uncertain significance	5	134686893	134686893	Human		name
597716254	CV3605508	single nucleotide variant	NM_021982.3(SEC24A):c.2779A>G (p.Met927Val)	not specified [RCV004861539]	uncertain significance	5	134715075	134715075	Human		name
597716272	CV3605510	single nucleotide variant	NM_021982.3(SEC24A):c.1160G>A (p.Arg387Gln)	not specified [RCV004861541]	uncertain significance	5	134676031	134676031	Human		name
597716282	CV3605511	single nucleotide variant	NM_021982.3(SEC24A):c.2989G>A (p.Gly997Arg)	not specified [RCV004861542]	uncertain significance	5	134721016	134721016	Human		name
597716301	CV3605513	single nucleotide variant	NM_021982.3(SEC24A):c.2056G>A (p.Ala686Thr)	not specified [RCV004861544]	uncertain significance	5	134697195	134697195	Human		name
597716308	CV3605515	single nucleotide variant	NM_021982.3(SEC24A):c.1534G>A (p.Val512Met)	not specified [RCV004861545]	uncertain significance	5	134686832	134686832	Human		name
597716326	CV3605517	single nucleotide variant	NM_021982.3(SEC24A):c.1318C>T (p.Pro440Ser)	not specified [RCV004861547]	uncertain significance	5	134679665	134679665	Human		name
597716344	CV3605519	single nucleotide variant	NM_021982.3(SEC24A):c.2864A>C (p.Glu955Ala)	not specified [RCV004861549]	uncertain significance	5	134715160	134715160	Human		name
597716365	CV3605521	single nucleotide variant	NM_021982.3(SEC24A):c.2738A>C (p.Gln913Pro)	not specified [RCV004861551]	uncertain significance	5	134715034	134715034	Human		name
598210884	CV3907183	single nucleotide variant	NM_021982.3(SEC24A):c.2219C>T (p.Thr740Ile)	not specified [RCV005270734]	uncertain significance	5	134698010	134698010	Human		name
598210891	CV3907184	single nucleotide variant	NM_021982.3(SEC24A):c.1187C>T (p.Thr396Met)	not specified [RCV005270735]	uncertain significance	5	134676058	134676058	Human		name
598210899	CV3907185	single nucleotide variant	NM_021982.3(SEC24A):c.2119C>T (p.Arg707Trp)	not specified [RCV005270736]	uncertain significance	5	134697910	134697910	Human		name
598210906	CV3907186	single nucleotide variant	NM_021982.3(SEC24A):c.2804T>C (p.Leu935Ser)	not specified [RCV005270737]	uncertain significance	5	134715100	134715100	Human		name
598210912	CV3907187	single nucleotide variant	NM_021982.3(SEC24A):c.2521C>G (p.Gln841Glu)	not specified [RCV005270738]	uncertain significance	5	134705407	134705407	Human		name
598210919	CV3907188	single nucleotide variant	NM_021982.3(SEC24A):c.1424G>C (p.Gly475Ala)	not specified [RCV005270739]	uncertain significance	5	134682415	134682415	Human		name
598210927	CV3907189	single nucleotide variant	NM_021982.3(SEC24A):c.1765A>G (p.Asn589Asp)	not specified [RCV005270740]	uncertain significance	5	134692643	134692643	Human		name
598210935	CV3907190	single nucleotide variant	NM_021982.3(SEC24A):c.2215C>T (p.Leu739Phe)	not specified [RCV005270741]	uncertain significance	5	134698006	134698006	Human		name
405705019	CV3310744	single nucleotide variant	NM_021982.3(SEC24A):c.3083A>G (p.Asp1028Gly)	not specified [RCV004447632]	uncertain significance	5	134723586	134723586	Human		name
405705034	CV3310746	single nucleotide variant	NM_021982.3(SEC24A):c.3262C>G (p.Gln1088Glu)	not specified [RCV004447634]	uncertain significance	5	134725074	134725074	Human		name
407492091	CV3476705	single nucleotide variant	NM_021982.3(SEC24A):c.3047C>T (p.Ser1016Leu)	not specified [RCV004667024]	likely benign	5	134721074	134721074	Human		name
407477097	CV3476708	single nucleotide variant	NM_021982.3(SEC24A):c.3008A>G (p.Asn1003Ser)	not specified [RCV004663637]	uncertain significance	5	134721035	134721035	Human		name

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