Sec16a Variant Search Result - Rat Genome Database

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283 records found for search term Sec16a

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401720446	CV2737247	single nucleotide variant	NM_014866.2(SEC16A):c.4647+2T>A	not provided [RCV003314186]	uncertain significance	9	136463461	136463461	Human		name
15104397	CV730621	single nucleotide variant	NM_014866.2(SEC16A):c.5551-9C>G	not provided [RCV000892875]	likely benign	9	136456175	136456175	Human		name
15154411	CV744476	single nucleotide variant	NM_014866.2(SEC16A):c.5074-8C>T	not provided [RCV000901949]	benign	9	136459882	136459882	Human		name
15158695	CV779312	single nucleotide variant	NM_014866.2(SEC16A):c.4991+8C>T	not provided [RCV000969567]	benign	9	136461169	136461169	Human		name
15146325	CV779582	single nucleotide variant	NM_014866.2(SEC16A):c.5410-7G>A	not provided [RCV000967143]	benign	9	136457591	136457591	Human		name
156206818	CV2382290	single nucleotide variant	NM_014866.2(SEC16A):c.26C>T (p.Pro9Leu)	not specified [RCV004230641]	uncertain significance	9	136477590	136477590	Human		name
15178603	CV711873	single nucleotide variant	NM_014866.2(SEC16A):c.249C>T (p.Pro83=)	not provided [RCV000973705]	benign	9	136477367	136477367	Human		name
15163440	CV737020	single nucleotide variant	NM_014866.2(SEC16A):c.126T>A (p.Ala42=)	not provided [RCV000903774]	likely benign	9	136477490	136477490	Human		name
156057919	CV2322891	single nucleotide variant	NM_014866.2(SEC16A):c.46C>T (p.Pro16Ser)	not specified [RCV004185344]	uncertain significance	9	136477570	136477570	Human		name
329360819	CV2439799	single nucleotide variant	NM_014866.2(SEC16A):c.87C>G (p.Ser29Arg)	not specified [RCV004255802]	uncertain significance	9	136477529	136477529	Human		name
407492006	CV3476637	single nucleotide variant	NM_014866.2(SEC16A):c.53C>T (p.Ala18Val)	not specified [RCV004667000]	uncertain significance	9	136477563	136477563	Human		name
407492013	CV3476641	single nucleotide variant	NM_014866.2(SEC16A):c.43C>T (p.Pro15Ser)	not specified [RCV004667002]	uncertain significance	9	136477573	136477573	Human		name
598210544	CV3907134	single nucleotide variant	NM_014866.2(SEC16A):c.86G>C (p.Ser29Thr)	not specified [RCV005270685]	uncertain significance	9	136477530	136477530	Human		name
15151543	CV711872	single nucleotide variant	NM_014866.2(SEC16A):c.696C>T (p.Cys232=)	not provided [RCV000968162]	benign	9	136476920	136476920	Human		name
155940478	CV2294083	single nucleotide variant	NM_014866.2(SEC16A):c.158A>C (p.Asp53Ala)	not specified [RCV004149460]	uncertain significance	9	136477458	136477458	Human		name
155979465	CV2339111	single nucleotide variant	NM_014866.2(SEC16A):c.128C>T (p.Pro43Leu)	not specified [RCV004187153]	uncertain significance	9	136477488	136477488	Human		name
155924458	CV2352078	single nucleotide variant	NM_014866.2(SEC16A):c.250G>A (p.Ala84Thr)	not specified [RCV004191173]	uncertain significance	9	136477366	136477366	Human		name
155966723	CV2396106	single nucleotide variant	NM_014866.2(SEC16A):c.191G>A (p.Ser64Asn)	not specified [RCV004237638]	likely benign	9	136477425	136477425	Human		name
401877055	CV2767810	single nucleotide variant	NM_014866.2(SEC16A):c.140C>T (p.Pro47Leu)	not specified [RCV004345931]	uncertain significance	9	136477476	136477476	Human		name
401895841	CV2768919	single nucleotide variant	NM_014866.2(SEC16A):c.106A>G (p.Asn36Asp)	not specified [RCV004347022]	uncertain significance	9	136477510	136477510	Human		name
401891021	CV2768920	single nucleotide variant	NM_014866.2(SEC16A):c.107A>C (p.Asn36Thr)	not specified [RCV004347023]	uncertain significance	9	136477509	136477509	Human		name
405704094	CV3310646	single nucleotide variant	NM_014866.2(SEC16A):c.155C>T (p.Thr52Met)	not specified [RCV004447534]	uncertain significance	9	136477461	136477461	Human		name
407492036	CV3476652	single nucleotide variant	NM_014866.2(SEC16A):c.251C>A (p.Ala84Glu)	not specified [RCV004667008]	uncertain significance	9	136477365	136477365	Human		name
407492048	CV3476657	single nucleotide variant	NM_014866.2(SEC16A):c.160C>G (p.Pro54Ala)	not specified [RCV004667011]	uncertain significance	9	136477456	136477456	Human		name
407492052	CV3476662	single nucleotide variant	NM_014866.2(SEC16A):c.109A>G (p.Asn37Asp)	not specified [RCV004667012]	uncertain significance	9	136477507	136477507	Human		name
15116145	CV711868	single nucleotide variant	NM_014866.2(SEC16A):c.2868T>C (p.Asn956=)	not provided [RCV000961983]	benign	9	136474748	136474748	Human		name
15162089	CV711869	single nucleotide variant	NM_014866.2(SEC16A):c.2130C>G (p.Ala710=)	not provided [RCV000970207]	benign	9	136475486	136475486	Human		name
15189951	CV723461	single nucleotide variant	NM_014866.2(SEC16A):c.1239C>T (p.Pro413=)	not provided [RCV000887966]	benign	9	136476377	136476377	Human		name
15135194	CV737017	single nucleotide variant	NM_014866.2(SEC16A):c.2454G>A (p.Pro818=)	not provided [RCV000898414]	likely benign	9	136475162	136475162	Human		name
15116246	CV737018	single nucleotide variant	NM_014866.2(SEC16A):c.1956C>T (p.Pro652=)	not provided [RCV000895166]	likely benign	9	136475660	136475660	Human		name
15122897	CV751564	single nucleotide variant	NM_014866.2(SEC16A):c.2892G>A (p.Val964=)	not provided [RCV000918728]	likely benign	9	136474724	136474724	Human		name
15151125	CV751565	single nucleotide variant	NM_014866.2(SEC16A):c.2532C>T (p.Asn844=)	not provided [RCV000923609]	likely benign	9	136475084	136475084	Human		name
15138546	CV767292	single nucleotide variant	NM_014866.2(SEC16A):c.1029A>G (p.Pro343=)	not provided [RCV000943413]	likely benign	9	136476587	136476587	Human		name
156320940	CV2197448	single nucleotide variant	NM_014866.2(SEC16A):c.537G>T (p.Met179Ile)	not specified [RCV004081183]	uncertain significance	9	136477079	136477079	Human		name
156138754	CV2202842	single nucleotide variant	NM_014866.2(SEC16A):c.367C>T (p.Pro123Ser)	not specified [RCV004073693]	uncertain significance	9	136477249	136477249	Human		name
156226383	CV2203127	single nucleotide variant	NM_014866.2(SEC16A):c.953G>A (p.Arg318Lys)	not specified [RCV004069366]	uncertain significance	9	136476663	136476663	Human		name
156334477	CV2214772	single nucleotide variant	NM_014866.2(SEC16A):c.618G>C (p.Gln206His)	not specified [RCV004090579]	uncertain significance	9	136476998	136476998	Human		name
155922292	CV2218817	single nucleotide variant	NM_014866.2(SEC16A):c.447G>T (p.Glu149Asp)	not specified [RCV004085062]	uncertain significance	9	136477169	136477169	Human		name
155916248	CV2239690	single nucleotide variant	NM_014866.2(SEC16A):c.641A>G (p.Gln214Arg)	not specified [RCV004108235]	uncertain significance	9	136476975	136476975	Human		name
156060262	CV2280118	single nucleotide variant	NM_014866.2(SEC16A):c.812C>G (p.Pro271Arg)	not specified [RCV004146771]	uncertain significance	9	136476804	136476804	Human		name
329360039	CV2462419	single nucleotide variant	NM_014866.2(SEC16A):c.769C>T (p.His257Tyr)	not specified [RCV004268175]	uncertain significance	9	136476847	136476847	Human		name
401770173	CV2719073	single nucleotide variant	NM_014866.2(SEC16A):c.528T>A (p.His176Gln)	not specified [RCV004322649]	likely benign	9	136477088	136477088	Human		name
401911194	CV2823608	single nucleotide variant	NM_014866.2(SEC16A):c.6297G>A (p.Thr2099=)	not provided [RCV003425868]	likely benign	9	136451271	136451271	Human		name
401918677	CV2823609	single nucleotide variant	NM_014866.2(SEC16A):c.5253T>C (p.Gly1751=)	not provided [RCV003430402]	likely benign	9	136459494	136459494	Human		name
401918679	CV2823610	single nucleotide variant	NM_014866.2(SEC16A):c.3792C>T (p.Tyr1264=)	not provided [RCV003430403]	likely benign	9	136468425	136468425	Human		name
405704303	CV3310673	single nucleotide variant	NM_014866.2(SEC16A):c.646G>C (p.Gly216Arg)	not specified [RCV004447561]	uncertain significance	9	136476970	136476970	Human		name
407492002	CV3476635	single nucleotide variant	NM_014866.2(SEC16A):c.604C>T (p.Pro202Ser)	not specified [RCV004666999]	uncertain significance	9	136477012	136477012	Human		name
407492044	CV3476655	single nucleotide variant	NM_014866.2(SEC16A):c.922A>G (p.Ile308Val)	not specified [RCV004667010]	likely benign	9	136476694	136476694	Human		name
407476950	CV3476656	single nucleotide variant	NM_014866.2(SEC16A):c.743C>T (p.Pro248Leu)	not specified [RCV004663600]	uncertain significance	9	136476873	136476873	Human		name
597715279	CV3605404	single nucleotide variant	NM_014866.2(SEC16A):c.706C>G (p.Pro236Ala)	not specified [RCV004861446]	uncertain significance	9	136476910	136476910	Human		name
597715292	CV3605405	single nucleotide variant	NM_014866.2(SEC16A):c.580G>A (p.Gly194Ser)	not specified [RCV004861447]	likely benign	9	136477036	136477036	Human		name
597715412	CV3605419	single nucleotide variant	NM_014866.2(SEC16A):c.821C>G (p.Ala274Gly)	not specified [RCV004861459]	uncertain significance	9	136476795	136476795	Human		name
597715495	CV3605427	single nucleotide variant	NM_014866.2(SEC16A):c.5460G>A (p.Thr1820=)	not specified [RCV004861467]	likely benign	9	136457534	136457534	Human		name
597715574	CV3605436	single nucleotide variant	NM_014866.2(SEC16A):c.307T>G (p.Ser103Ala)	not specified [RCV004861475]	uncertain significance	9	136477309	136477309	Human		name
597715640	CV3605443	single nucleotide variant	NM_014866.2(SEC16A):c.656A>C (p.Gln219Pro)	not specified [RCV004861481]	uncertain significance	9	136476960	136476960	Human		name
597715673	CV3605446	single nucleotide variant	NM_014866.2(SEC16A):c.527A>G (p.His176Arg)	not specified [RCV004861484]	uncertain significance	9	136477089	136477089	Human		name
598210430	CV3907117	single nucleotide variant	NM_014866.2(SEC16A):c.988G>A (p.Ala330Thr)	not specified [RCV005270668]	likely benign	9	136476628	136476628	Human		name
598210513	CV3907129	single nucleotide variant	NM_014866.2(SEC16A):c.731C>T (p.Ala244Val)	not specified [RCV005270680]	uncertain significance	9	136476885	136476885	Human		name
15116138	CV711864	single nucleotide variant	NM_014866.2(SEC16A):c.7020C>T (p.Ser2340=)	not provided [RCV000961982]	benign	9	136441809	136441809	Human		name
15173339	CV711866	single nucleotide variant	NM_014866.2(SEC16A):c.4269C>T (p.Tyr1423=)	not provided [RCV000972595]	likely benign	9	136465996	136465996	Human		name
15116153	CV711871	single nucleotide variant	NM_014866.2(SEC16A):c.962C>T (p.Pro321Leu)	not provided [RCV000961984]	benign	9	136476654	136476654	Human		name
15122879	CV751561	single nucleotide variant	NM_014866.2(SEC16A):c.6645C>T (p.Val2215=)	not provided [RCV000918725]	likely benign	9	136447279	136447279	Human		name
15122892	CV751563	single nucleotide variant	NM_014866.2(SEC16A):c.4032C>T (p.Asp1344=)	not provided [RCV000918727]	likely benign	9	136466360	136466360	Human		name
156271384	CV2195234	single nucleotide variant	NM_014866.2(SEC16A):c.1885G>A (p.Ala629Thr)	not specified [RCV004080170]	uncertain significance	9	136475731	136475731	Human		name
156400032	CV2198921	single nucleotide variant	NM_014866.2(SEC16A):c.1346C>T (p.Pro449Leu)	not specified [RCV004078297]	uncertain significance	9	136476270	136476270	Human		name
156229372	CV2209355	single nucleotide variant	NM_014866.2(SEC16A):c.2490T>G (p.Ile830Met)	not specified [RCV004093530]	uncertain significance	9	136475126	136475126	Human		name
156043154	CV2215827	single nucleotide variant	NM_014866.2(SEC16A):c.1361C>T (p.Ser454Leu)	not specified [RCV004096939]	uncertain significance	9	136476255	136476255	Human		name
156280256	CV2224111	single nucleotide variant	NM_014866.2(SEC16A):c.2062A>G (p.Met688Val)	not specified [RCV004095974]	likely benign	9	136475554	136475554	Human		name
156236277	CV2224112	single nucleotide variant	NM_014866.2(SEC16A):c.2074G>A (p.Ala692Thr)	not specified [RCV004095975]	likely benign	9	136475542	136475542	Human		name
156178830	CV2229431	single nucleotide variant	NM_014866.2(SEC16A):c.1570A>G (p.Ser524Gly)	not specified [RCV004101205]	likely benign	9	136476046	136476046	Human		name
156063133	CV2272336	single nucleotide variant	NM_014866.2(SEC16A):c.2512A>G (p.Asn838Asp)	not specified [RCV004131480]	uncertain significance	9	136475104	136475104	Human		name
155991056	CV2276542	single nucleotide variant	NM_014866.2(SEC16A):c.1979A>G (p.Glu660Gly)	not specified [RCV004146042]	uncertain significance	9	136475637	136475637	Human		name
155924008	CV2280440	single nucleotide variant	NM_014866.2(SEC16A):c.2506A>G (p.Ser836Gly)	not specified [RCV004140612]	uncertain significance	9	136475110	136475110	Human		name
156287467	CV2288398	single nucleotide variant	NM_014866.2(SEC16A):c.1211G>C (p.Cys404Ser)	not specified [RCV004151949]	likely benign	9	136476405	136476405	Human		name
156160167	CV2311647	single nucleotide variant	NM_014866.2(SEC16A):c.1804A>G (p.Ile602Val)	not specified [RCV004168742]	likely benign	9	136475812	136475812	Human		name
156259243	CV2322214	single nucleotide variant	NM_014866.2(SEC16A):c.2762C>G (p.Pro921Arg)	not specified [RCV004175988]	uncertain significance	9	136474854	136474854	Human		name
155919181	CV2333150	single nucleotide variant	NM_014866.2(SEC16A):c.1819G>A (p.Ala607Thr)	not specified [RCV004194440]	uncertain significance	9	136475797	136475797	Human		name
156183430	CV2339315	single nucleotide variant	NM_014866.2(SEC16A):c.2419G>A (p.Ala807Thr)	not specified [RCV004191547]	uncertain significance	9	136475197	136475197	Human		name
156331514	CV2339650	single nucleotide variant	NM_014866.2(SEC16A):c.2069C>T (p.Pro690Leu)	not specified [RCV004196357]	uncertain significance	9	136475547	136475547	Human		name
155985207	CV2344498	single nucleotide variant	NM_014866.2(SEC16A):c.2234C>T (p.Pro745Leu)	not specified [RCV004195238]	uncertain significance	9	136475382	136475382	Human		name
156054662	CV2361260	single nucleotide variant	NM_014866.2(SEC16A):c.2851C>T (p.Leu951Phe)	not specified [RCV004218478]	uncertain significance	9	136474765	136474765	Human		name
156260171	CV2381103	single nucleotide variant	NM_014866.2(SEC16A):c.2929G>T (p.Asp977Tyr)	not specified [RCV004225136]	uncertain significance	9	136474687	136474687	Human		name
156070557	CV2381325	single nucleotide variant	NM_014866.2(SEC16A):c.1915T>A (p.Cys639Ser)	not specified [RCV004227384]	uncertain significance	9	136475701	136475701	Human		name
156104863	CV2386986	single nucleotide variant	NM_014866.2(SEC16A):c.2698A>G (p.Ser900Gly)	not specified [RCV004226741]	uncertain significance	9	136474918	136474918	Human		name
156114626	CV2397192	single nucleotide variant	NM_014866.2(SEC16A):c.1948G>A (p.Ala650Thr)	not specified [RCV004238732]	uncertain significance	9	136475668	136475668	Human		name
156228825	CV2400121	single nucleotide variant	NM_014866.2(SEC16A):c.2237C>T (p.Ala746Val)	not specified [RCV004242926]	uncertain significance	9	136475379	136475379	Human		name
329368759	CV2424622	single nucleotide variant	NM_014866.2(SEC16A):c.1012G>A (p.Ala338Thr)	not specified [RCV004254498]	likely benign	9	136476604	136476604	Human		name
329391239	CV2447923	single nucleotide variant	NM_014866.2(SEC16A):c.1838C>T (p.Pro613Leu)	not specified [RCV004260732]	uncertain significance	9	136475778	136475778	Human		name
329389165	CV2448635	single nucleotide variant	NM_014866.2(SEC16A):c.2626G>A (p.Gly876Ser)	not specified [RCV004259305]	likely benign	9	136474990	136474990	Human		name
329351951	CV2455522	single nucleotide variant	NM_014866.2(SEC16A):c.2893G>C (p.Val965Leu)	not specified [RCV004276785]	uncertain significance	9	136474723	136474723	Human		name
401739295	CV2673260	single nucleotide variant	NM_014866.2(SEC16A):c.2168C>T (p.Thr723Met)	not specified [RCV004286063]	uncertain significance	9	136475448	136475448	Human		name
401768241	CV2675182	single nucleotide variant	NM_014866.2(SEC16A):c.1787C>T (p.Pro596Leu)	not specified [RCV004289955]	uncertain significance	9	136475829	136475829	Human		name
401726166	CV2699134	single nucleotide variant	NM_014866.2(SEC16A):c.1996A>T (p.Met666Leu)	not specified [RCV004303637]	uncertain significance	9	136475620	136475620	Human		name
401737840	CV2703668	single nucleotide variant	NM_014866.2(SEC16A):c.1122G>A (p.Met374Ile)	not specified [RCV004315922]	uncertain significance	9	136476494	136476494	Human		name
401735131	CV2706679	single nucleotide variant	NM_014866.2(SEC16A):c.1952T>G (p.Leu651Arg)	not specified [RCV004319253]	uncertain significance	9	136475664	136475664	Human		name
401751786	CV2727143	single nucleotide variant	NM_014866.2(SEC16A):c.1817G>A (p.Ser606Asn)	not specified [RCV004325502]	uncertain significance	9	136475799	136475799	Human		name
401880695	CV2770068	single nucleotide variant	NM_014866.2(SEC16A):c.1504G>C (p.Ala502Pro)	not specified [RCV004353882]	uncertain significance	9	136476112	136476112	Human		name
401898423	CV2787890	single nucleotide variant	NM_014866.2(SEC16A):c.1859G>A (p.Gly620Glu)	not specified [RCV004358567]	uncertain significance	9	136475757	136475757	Human		name
401918681	CV2823611	single nucleotide variant	NM_014866.2(SEC16A):c.2252C>G (p.Ala751Gly)	not provided [RCV003430404]	likely benign	9	136475364	136475364	Human		name
401944906	CV2840724	single nucleotide variant	NM_014866.2(SEC16A):c.2660G>A (p.Gly887Glu)	not provided [RCV003457579]	likely benign	9	136474956	136474956	Human		name
405704067	CV3310643	single nucleotide variant	NM_014866.2(SEC16A):c.1006C>T (p.Pro336Ser)	not specified [RCV004447531]	uncertain significance	9	136476610	136476610	Human		name
405704079	CV3310644	single nucleotide variant	NM_014866.2(SEC16A):c.1204G>A (p.Asp402Asn)	not specified [RCV004447532]	uncertain significance	9	136476412	136476412	Human		name
405704086	CV3310645	single nucleotide variant	NM_014866.2(SEC16A):c.1232G>A (p.Arg411His)	not specified [RCV004447533]	likely benign	9	136476384	136476384	Human		name
405704100	CV3310647	single nucleotide variant	NM_014866.2(SEC16A):c.2333C>T (p.Pro778Leu)	not specified [RCV004447535]	uncertain significance	9	136475283	136475283	Human		name
405704108	CV3310648	single nucleotide variant	NM_014866.2(SEC16A):c.2391G>A (p.Met797Ile)	not specified [RCV004447536]	uncertain significance	9	136475225	136475225	Human		name
405704113	CV3310649	single nucleotide variant	NM_014866.2(SEC16A):c.2474A>G (p.Asn825Ser)	not specified [RCV004447537]	uncertain significance	9	136475142	136475142	Human		name
405704126	CV3310651	single nucleotide variant	NM_014866.2(SEC16A):c.2555C>G (p.Ser852Cys)	not specified [RCV004447539]	uncertain significance	9	136475061	136475061	Human		name
405704134	CV3310652	single nucleotide variant	NM_014866.2(SEC16A):c.2573C>G (p.Ser858Cys)	not specified [RCV004447540]	uncertain significance	9	136475043	136475043	Human		name
405704140	CV3310653	single nucleotide variant	NM_014866.2(SEC16A):c.2712A>T (p.Gln904His)	not specified [RCV004447541]	uncertain significance	9	136474904	136474904	Human		name
405704152	CV3310654	single nucleotide variant	NM_014866.2(SEC16A):c.2732C>G (p.Ser911Cys)	not specified [RCV004447542]	uncertain significance	9	136474884	136474884	Human		name
407476922	CV3476642	single nucleotide variant	NM_014866.2(SEC16A):c.1267C>T (p.Leu423Phe)	not specified [RCV004663594]	uncertain significance	9	136476349	136476349	Human		name
407476936	CV3476646	single nucleotide variant	NM_014866.2(SEC16A):c.1255G>A (p.Gly419Arg)	not specified [RCV004663597]	uncertain significance	9	136476361	136476361	Human		name
407492040	CV3476654	single nucleotide variant	NM_014866.2(SEC16A):c.2348G>A (p.Gly783Asp)	not specified [RCV004667009]	likely benign	9	136475268	136475268	Human		name
408377951	CV3500886	single nucleotide variant	NM_014866.2(SEC16A):c.1519G>A (p.Gly507Arg)	not provided [RCV004722536]	likely benign	9	136476097	136476097	Human		name
597715343	CV3605411	single nucleotide variant	NM_014866.2(SEC16A):c.1789C>T (p.Pro597Ser)	not specified [RCV004861452]	uncertain significance	9	136475827	136475827	Human		name
597715401	CV3605418	single nucleotide variant	NM_014866.2(SEC16A):c.2498C>T (p.Pro833Leu)	not specified [RCV004861458]	uncertain significance	9	136475118	136475118	Human		name
597715424	CV3605420	single nucleotide variant	NM_014866.2(SEC16A):c.2157G>C (p.Glu719Asp)	not specified [RCV004861460]	uncertain significance	9	136475459	136475459	Human		name
597715433	CV3605421	single nucleotide variant	NM_014866.2(SEC16A):c.2695C>T (p.Pro899Ser)	not specified [RCV004861461]	uncertain significance	9	136474921	136474921	Human		name
597715483	CV3605426	single nucleotide variant	NM_014866.2(SEC16A):c.2026C>T (p.Pro676Ser)	not specified [RCV004861466]	uncertain significance	9	136475590	136475590	Human		name
597715545	CV3605433	single nucleotide variant	NM_014866.2(SEC16A):c.2543C>T (p.Ser848Phe)	not specified [RCV004861472]	uncertain significance	9	136475073	136475073	Human		name
597715584	CV3605437	single nucleotide variant	NM_014866.2(SEC16A):c.1753C>T (p.Arg585Cys)	not specified [RCV004861476]	uncertain significance	9	136475863	136475863	Human		name
597715595	CV3605438	single nucleotide variant	NM_014866.2(SEC16A):c.1459T>A (p.Phe487Ile)	not specified [RCV004861477]	uncertain significance	9	136476157	136476157	Human		name
597715618	CV3605441	single nucleotide variant	NM_014866.2(SEC16A):c.2603C>T (p.Pro868Leu)	not specified [RCV004861479]	uncertain significance	9	136475013	136475013	Human		name
597715661	CV3605445	single nucleotide variant	NM_014866.2(SEC16A):c.2573C>T (p.Ser858Phe)	not specified [RCV004861483]	uncertain significance	9	136475043	136475043	Human		name
598210401	CV3907112	single nucleotide variant	NM_014866.2(SEC16A):c.1598T>G (p.Leu533Arg)	not specified [RCV005270663]	uncertain significance	9	136476018	136476018	Human		name
598210456	CV3907121	single nucleotide variant	NM_014866.2(SEC16A):c.2009G>A (p.Cys670Tyr)	not specified [RCV005270672]	uncertain significance	9	136475607	136475607	Human		name
598210464	CV3907122	single nucleotide variant	NM_014866.2(SEC16A):c.2299G>A (p.Gly767Arg)	not specified [RCV005270673]	uncertain significance	9	136475317	136475317	Human		name
598210471	CV3907123	single nucleotide variant	NM_014866.2(SEC16A):c.2779C>G (p.Gln927Glu)	not specified [RCV005270674]	uncertain significance	9	136474837	136474837	Human		name
598210486	CV3907125	single nucleotide variant	NM_014866.2(SEC16A):c.2281C>T (p.Pro761Ser)	not specified [RCV005270676]	uncertain significance	9	136475335	136475335	Human		name
598210493	CV3907126	single nucleotide variant	NM_014866.2(SEC16A):c.1252G>T (p.Val418Leu)	not specified [RCV005270677]	uncertain significance	9	136476364	136476364	Human		name
598210520	CV3907130	single nucleotide variant	NM_014866.2(SEC16A):c.1967C>T (p.Pro656Leu)	not specified [RCV005270681]	uncertain significance	9	136475649	136475649	Human		name
598210527	CV3907131	single nucleotide variant	NM_014866.2(SEC16A):c.2840C>T (p.Ala947Val)	not specified [RCV005270682]	uncertain significance	9	136474776	136474776	Human		name
598210533	CV3907132	single nucleotide variant	NM_014866.2(SEC16A):c.2543C>G (p.Ser848Cys)	not specified [RCV005270683]	uncertain significance	9	136475073	136475073	Human		name
598210540	CV3907133	single nucleotide variant	NM_014866.2(SEC16A):c.1729G>A (p.Glu577Lys)	not specified [RCV005270684]	uncertain significance	9	136475887	136475887	Human		name
598210550	CV3907135	single nucleotide variant	NM_014866.2(SEC16A):c.2627G>A (p.Gly876Asp)	not specified [RCV005270686]	uncertain significance	9	136474989	136474989	Human		name
598210571	CV3907138	single nucleotide variant	NM_014866.2(SEC16A):c.1061G>A (p.Gly354Glu)	not specified [RCV005270689]	uncertain significance	9	136476555	136476555	Human		name
15178599	CV711870	single nucleotide variant	NM_014866.2(SEC16A):c.1178G>A (p.Gly393Asp)	not provided [RCV000973704]	benign	9	136476438	136476438	Human		name
15182787	CV723460	single nucleotide variant	NM_014866.2(SEC16A):c.2977G>A (p.Ala993Thr)	not provided [RCV000886075]	likely benign	9	136474639	136474639	Human		name
15148000	CV737019	single nucleotide variant	NM_014866.2(SEC16A):c.1081C>T (p.Pro361Ser)	not provided [RCV000900632]	likely benign	9	136476535	136476535	Human		name
150495154	CV1225021	single nucleotide variant	NM_014866.2(SEC16A):c.3115C>T (p.Arg1039Cys)	not provided [RCV001619499]	benign	9	136474501	136474501	Human	6	name
150495154	CV1225021	single nucleotide variant	NM_014866.2(SEC16A):c.3115C>T (p.Arg1039Cys)	not provided [RCV001619499]	benign	9	136474501	136474502	Human	6	name
155926200	CV2208131	single nucleotide variant	NM_014866.2(SEC16A):c.4058C>T (p.Ser1353Leu)	not specified [RCV004086811]	uncertain significance	9	136466334	136466334	Human		name
155964600	CV2210014	single nucleotide variant	NM_014866.2(SEC16A):c.4843G>A (p.Glu1615Lys)	not specified [RCV004076447]	uncertain significance	9	136462937	136462937	Human		name
156335384	CV2211458	single nucleotide variant	NM_014866.2(SEC16A):c.4270C>T (p.Pro1424Ser)	not specified [RCV004090685]	uncertain significance	9	136465995	136465995	Human		name
156128759	CV2220073	single nucleotide variant	NM_014866.2(SEC16A):c.4207T>C (p.Phe1403Leu)	not specified [RCV004093947]	uncertain significance	9	136466058	136466058	Human		name
156234942	CV2224000	single nucleotide variant	NM_014866.2(SEC16A):c.3443C>T (p.Ala1148Val)	not specified [RCV004094249]	uncertain significance	9	136474173	136474173	Human		name
155930353	CV2224720	single nucleotide variant	NM_014866.2(SEC16A):c.4081C>A (p.His1361Asn)	not specified [RCV004092554]	uncertain significance	9	136466311	136466311	Human		name
155997638	CV2250576	single nucleotide variant	NM_014866.2(SEC16A):c.6533C>T (p.Pro2178Leu)	not specified [RCV004129220]	uncertain significance	9	136447595	136447595	Human		name
156071768	CV2267348	single nucleotide variant	NM_014866.2(SEC16A):c.4166C>T (p.Ser1389Phe)	not specified [RCV004134008]	uncertain significance	9	136466099	136466099	Human		name
156048746	CV2271748	single nucleotide variant	NM_014866.2(SEC16A):c.6497C>G (p.Ala2166Gly)	not specified [RCV004130593]	uncertain significance	9	136447631	136447631	Human		name
156019358	CV2272592	single nucleotide variant	NM_014866.2(SEC16A):c.6901C>G (p.Arg2301Gly)	not specified [RCV004133478]	uncertain significance	9	136445078	136445078	Human		name
156275198	CV2279934	single nucleotide variant	NM_014866.2(SEC16A):c.4855G>C (p.Glu1619Gln)	not specified [RCV004146309]	uncertain significance	9	136462925	136462925	Human		name
156035256	CV2282964	single nucleotide variant	NM_014866.2(SEC16A):c.3350C>G (p.Pro1117Arg)	not specified [RCV004143599]	uncertain significance	9	136474266	136474266	Human		name
156063732	CV2287003	single nucleotide variant	NM_014866.2(SEC16A):c.5065G>A (p.Ala1689Thr)	not specified [RCV004144891]	uncertain significance	9	136460050	136460050	Human		name
156285133	CV2289038	single nucleotide variant	NM_014866.2(SEC16A):c.3101C>T (p.Ala1034Val)	not specified [RCV004149985]	uncertain significance	9	136474515	136474515	Human		name
156265220	CV2299102	single nucleotide variant	NM_014866.2(SEC16A):c.5957G>A (p.Cys1986Tyr)	not specified [RCV004152460]	likely benign	9	136454228	136454228	Human		name
155911415	CV2303814	single nucleotide variant	NM_014866.2(SEC16A):c.4039A>G (p.Ser1347Gly)	not specified [RCV004163653]	uncertain significance	9	136466353	136466353	Human		name
156257793	CV2322093	single nucleotide variant	NM_014866.2(SEC16A):c.4834A>G (p.Ser1612Gly)	not specified [RCV004173835]	uncertain significance	9	136462946	136462946	Human		name
156178360	CV2327392	single nucleotide variant	NM_014866.2(SEC16A):c.6977C>G (p.Pro2326Arg)	not specified [RCV004174817]	uncertain significance	9	136443851	136443851	Human		name
156263537	CV2329382	single nucleotide variant	NM_014866.2(SEC16A):c.4262A>G (p.Tyr1421Cys)	not specified [RCV004187396]	uncertain significance	9	136466003	136466003	Human		name
155921299	CV2350643	single nucleotide variant	NM_014866.2(SEC16A):c.3266C>T (p.Ala1089Val)	not specified [RCV004204982]	uncertain significance	9	136474350	136474350	Human		name
156141062	CV2358376	single nucleotide variant	NM_014866.2(SEC16A):c.3641G>A (p.Arg1214His)	not specified [RCV004207271]	uncertain significance	9	136472038	136472038	Human		name
155929177	CV2363459	single nucleotide variant	NM_014866.2(SEC16A):c.7025G>A (p.Ser2342Asn)	not specified [RCV004216034]	uncertain significance	9	136441804	136441804	Human		name
155930575	CV2366827	single nucleotide variant	NM_014866.2(SEC16A):c.6872C>T (p.Ser2291Leu)	not specified [RCV004210815]	uncertain significance	9	136445107	136445107	Human		name
155929545	CV2369772	single nucleotide variant	NM_014866.2(SEC16A):c.3617C>T (p.Ala1206Val)	not specified [RCV004215159]	uncertain significance	9	136472062	136472062	Human		name
156138380	CV2374214	single nucleotide variant	NM_014866.2(SEC16A):c.6503C>T (p.Pro2168Leu)	not specified [RCV004229358]	uncertain significance	9	136447625	136447625	Human		name
156388740	CV2376028	single nucleotide variant	NM_014866.2(SEC16A):c.3488G>A (p.Arg1163Gln)	not specified [RCV004220273]	uncertain significance	9	136474128	136474128	Human		name
156349157	CV2376480	single nucleotide variant	NM_014866.2(SEC16A):c.3821G>A (p.Arg1274His)	not specified [RCV004220655]	uncertain significance	9	136467065	136467065	Human		name
156151992	CV2377594	single nucleotide variant	NM_014866.2(SEC16A):c.4271C>T (p.Pro1424Leu)	not specified [RCV004227784]	uncertain significance	9	136465994	136465994	Human		name
156170313	CV2380578	single nucleotide variant	NM_014866.2(SEC16A):c.3163G>A (p.Glu1055Lys)	not specified [RCV004224900]	uncertain significance	9	136474453	136474453	Human		name
155927909	CV2391570	single nucleotide variant	NM_014866.2(SEC16A):c.5731G>A (p.Glu1911Lys)	not specified [RCV004239950]	uncertain significance	9	136455727	136455727	Human		name
156099014	CV2392832	single nucleotide variant	NM_014866.2(SEC16A):c.3866G>A (p.Arg1289Gln)	not specified [RCV004247191]	uncertain significance	9	136467020	136467020	Human		name
156260955	CV2395588	single nucleotide variant	NM_014866.2(SEC16A):c.5692G>A (p.Gly1898Arg)	not specified [RCV004241439]	uncertain significance	9	136455766	136455766	Human		name
155931799	CV2399905	single nucleotide variant	NM_014866.2(SEC16A):c.6182A>G (p.Asp2061Gly)	not specified [RCV004246846]	uncertain significance	9	136451386	136451386	Human		name
329372547	CV2424130	single nucleotide variant	NM_014866.2(SEC16A):c.4034G>A (p.Arg1345Gln)	not specified [RCV004248029]	uncertain significance	9	136466358	136466358	Human		name
329356148	CV2430604	single nucleotide variant	NM_014866.2(SEC16A):c.6193C>T (p.Pro2065Ser)	not specified [RCV004253798]	uncertain significance	9	136451375	136451375	Human		name
329360894	CV2439863	single nucleotide variant	NM_014866.2(SEC16A):c.4147C>T (p.His1383Tyr)	not specified [RCV004257903]	uncertain significance	9	136466118	136466118	Human		name
329400157	CV2440693	single nucleotide variant	NM_014866.2(SEC16A):c.5197A>G (p.Arg1733Gly)	not specified [RCV004258644]	uncertain significance	9	136459550	136459550	Human		name
329374281	CV2443816	single nucleotide variant	NM_014866.2(SEC16A):c.3476A>T (p.Tyr1159Phe)	not specified [RCV004258156]	uncertain significance	9	136474140	136474140	Human		name
329380312	CV2444320	single nucleotide variant	NM_014866.2(SEC16A):c.3163G>C (p.Glu1055Gln)	not specified [RCV004263079]	uncertain significance	9	136474453	136474453	Human		name
329391000	CV2447605	single nucleotide variant	NM_014866.2(SEC16A):c.3760G>A (p.Asp1254Asn)	not specified [RCV004258410]	uncertain significance	9	136468457	136468457	Human		name
329391435	CV2448555	single nucleotide variant	NM_014866.2(SEC16A):c.6874C>T (p.Arg2292Cys)	not specified [RCV004259235]	uncertain significance	9	136445105	136445105	Human		name
329373801	CV2452675	single nucleotide variant	NM_014866.2(SEC16A):c.6248C>T (p.Ser2083Leu)	not specified [RCV004275238]	uncertain significance	9	136451320	136451320	Human		name
329387874	CV2471063	single nucleotide variant	NM_014866.2(SEC16A):c.6253G>C (p.Ala2085Pro)	not specified [RCV004278019]	uncertain significance	9	136451315	136451315	Human		name
401732584	CV2675129	single nucleotide variant	NM_014866.2(SEC16A):c.3022G>A (p.Val1008Met)	not specified [RCV004289909]	likely benign	9	136474594	136474594	Human		name
401741032	CV2690356	single nucleotide variant	NM_014866.2(SEC16A):c.4831G>A (p.Ala1611Thr)	not specified [RCV004302351]	likely benign	9	136462949	136462949	Human		name
401758402	CV2694085	single nucleotide variant	NM_014866.2(SEC16A):c.6910A>T (p.Ser2304Cys)	not specified [RCV004302519]	uncertain significance	9	136445069	136445069	Human		name
401761884	CV2699444	single nucleotide variant	NM_014866.2(SEC16A):c.6497C>T (p.Ala2166Val)	not specified [RCV004299668]	uncertain significance	9	136447631	136447631	Human		name
401782930	CV2707612	single nucleotide variant	NM_014866.2(SEC16A):c.7067T>C (p.Leu2356Pro)	not specified [RCV004306553]	uncertain significance	9	136441762	136441762	Human		name
401777517	CV2708071	single nucleotide variant	NM_014866.2(SEC16A):c.4078G>A (p.Ala1360Thr)	not specified [RCV004309313]	uncertain significance	9	136466314	136466314	Human		name
401762664	CV2714228	single nucleotide variant	NM_014866.2(SEC16A):c.3364G>T (p.Val1122Leu)	not specified [RCV004317456]	uncertain significance	9	136474252	136474252	Human		name
401762668	CV2714229	single nucleotide variant	NM_014866.2(SEC16A):c.6628G>A (p.Ala2210Thr)	not specified [RCV004317457]	uncertain significance	9	136447296	136447296	Human		name
401750949	CV2715819	single nucleotide variant	NM_014866.2(SEC16A):c.6656C>G (p.Ala2219Gly)	not specified [RCV004328942]	uncertain significance	9	136447268	136447268	Human		name
401723302	CV2724843	single nucleotide variant	NM_014866.2(SEC16A):c.4939C>G (p.Leu1647Val)	not specified [RCV004317837]	uncertain significance	9	136461229	136461229	Human		name
401769146	CV2734651	single nucleotide variant	NM_014866.2(SEC16A):c.5861C>T (p.Pro1954Leu)	not specified [RCV004333610]	uncertain significance	9	136454324	136454324	Human		name
401720442	CV2737246	single nucleotide variant	NM_014866.2(SEC16A):c.5255T>C (p.Val1752Ala)	not provided [RCV003314185]	uncertain significance	9	136459492	136459492	Human		name
401866437	CV2762644	single nucleotide variant	NM_014866.2(SEC16A):c.3284A>G (p.Asn1095Ser)	not specified [RCV004340206]	uncertain significance	9	136474332	136474332	Human		name
401890025	CV2763596	single nucleotide variant	NM_014866.2(SEC16A):c.6911G>C (p.Ser2304Thr)	not specified [RCV004343105]	uncertain significance	9	136445068	136445068	Human		name
401893577	CV2765354	single nucleotide variant	NM_014866.2(SEC16A):c.4247C>T (p.Pro1416Leu)	not specified [RCV004339862]	uncertain significance	9	136466018	136466018	Human		name
401863777	CV2770823	single nucleotide variant	NM_014866.2(SEC16A):c.4318A>G (p.Thr1440Ala)	not specified [RCV004349855]	uncertain significance	9	136464548	136464548	Human		name
401862203	CV2775194	single nucleotide variant	NM_014866.2(SEC16A):c.6259G>A (p.Glu2087Lys)	not specified [RCV004346538]	uncertain significance	9	136451309	136451309	Human		name
405704159	CV3310655	single nucleotide variant	NM_014866.2(SEC16A):c.3143C>T (p.Ala1048Val)	not specified [RCV004447543]	uncertain significance	9	136474473	136474473	Human		name
405704166	CV3310656	single nucleotide variant	NM_014866.2(SEC16A):c.3176A>G (p.Gln1059Arg)	not specified [RCV004447544]	uncertain significance	9	136474440	136474440	Human		name
405704174	CV3310657	single nucleotide variant	NM_014866.2(SEC16A):c.3556C>T (p.Leu1186Phe)	not specified [RCV004447545]	uncertain significance	9	136474060	136474060	Human		name
405704181	CV3310658	single nucleotide variant	NM_014866.2(SEC16A):c.3640C>T (p.Arg1214Cys)	not specified [RCV004447546]	uncertain significance	9	136472039	136472039	Human		name
405704188	CV3310659	single nucleotide variant	NM_014866.2(SEC16A):c.3805C>A (p.Pro1269Thr)	not specified [RCV004447547]	uncertain significance	9	136467081	136467081	Human		name
405704195	CV3310660	single nucleotide variant	NM_014866.2(SEC16A):c.3977G>T (p.Gly1326Val)	not specified [RCV004447548]	uncertain significance	9	136466415	136466415	Human		name
405704201	CV3310661	single nucleotide variant	NM_014866.2(SEC16A):c.4013C>T (p.Pro1338Leu)	not specified [RCV004447549]	uncertain significance	9	136466379	136466379	Human		name
405704209	CV3310662	single nucleotide variant	NM_014866.2(SEC16A):c.4033C>T (p.Arg1345Trp)	not specified [RCV004447550]	uncertain significance	9	136466359	136466359	Human		name
405704229	CV3310664	single nucleotide variant	NM_014866.2(SEC16A):c.4114T>C (p.Ser1372Pro)	not specified [RCV004447552]	uncertain significance	9	136466278	136466278	Human		name
405704236	CV3310665	single nucleotide variant	NM_014866.2(SEC16A):c.4132C>G (p.Gln1378Glu)	not specified [RCV004447553]	uncertain significance	9	136466133	136466133	Human		name
405704246	CV3310666	single nucleotide variant	NM_014866.2(SEC16A):c.4178C>T (p.Pro1393Leu)	not specified [RCV004447554]	uncertain significance	9	136466087	136466087	Human		name
405704256	CV3310667	single nucleotide variant	NM_014866.2(SEC16A):c.4198C>G (p.His1400Asp)	not specified [RCV004447555]	uncertain significance	9	136466067	136466067	Human		name
405704262	CV3310668	single nucleotide variant	NM_014866.2(SEC16A):c.4583T>C (p.Leu1528Ser)	not specified [RCV004447556]	uncertain significance	9	136463527	136463527	Human		name
405704269	CV3310669	single nucleotide variant	NM_014866.2(SEC16A):c.5152G>A (p.Val1718Ile)	not specified [RCV004447557]	uncertain significance	9	136459796	136459796	Human		name
405704278	CV3310670	single nucleotide variant	NM_014866.2(SEC16A):c.5551A>T (p.Met1851Leu)	not specified [RCV004447558]	uncertain significance	9	136456166	136456166	Human		name
405704286	CV3310671	single nucleotide variant	NM_014866.2(SEC16A):c.5609C>G (p.Ser1870Cys)	not specified [RCV004447559]	uncertain significance	9	136456108	136456108	Human		name
405704297	CV3310672	single nucleotide variant	NM_014866.2(SEC16A):c.6097C>A (p.Pro2033Thr)	not specified [RCV004447560]	uncertain significance	9	136453490	136453490	Human		name
405704310	CV3310674	single nucleotide variant	NM_014866.2(SEC16A):c.6655G>A (p.Ala2219Thr)	not specified [RCV004447562]	uncertain significance	9	136447269	136447269	Human		name
405704318	CV3310675	single nucleotide variant	NM_014866.2(SEC16A):c.6740G>A (p.Gly2247Glu)	not specified [RCV004447563]	uncertain significance	9	136446907	136446907	Human		name
405704327	CV3310676	single nucleotide variant	NM_014866.2(SEC16A):c.6937G>A (p.Asp2313Asn)	not specified [RCV004447564]	uncertain significance	9	136443891	136443891	Human		name
407476905	CV3476634	single nucleotide variant	NM_014866.2(SEC16A):c.5567G>A (p.Arg1856Gln)	not specified [RCV004663590]	uncertain significance	9	136456150	136456150	Human		name
407476909	CV3476636	single nucleotide variant	NM_014866.2(SEC16A):c.3487C>T (p.Arg1163Trp)	not specified [RCV004663591]	uncertain significance	9	136474129	136474129	Human		name
407492010	CV3476639	single nucleotide variant	NM_014866.2(SEC16A):c.4697C>T (p.Thr1566Ile)	not specified [RCV004667001]	uncertain significance	9	136463083	136463083	Human		name
407476918	CV3476640	single nucleotide variant	NM_014866.2(SEC16A):c.6902G>A (p.Arg2301His)	not specified [RCV004663593]	uncertain significance	9	136445077	136445077	Human		name
407476926	CV3476643	single nucleotide variant	NM_014866.2(SEC16A):c.7041G>C (p.Arg2347Ser)	not specified [RCV004663595]	uncertain significance	9	136441788	136441788	Human		name
407492016	CV3476644	single nucleotide variant	NM_014866.2(SEC16A):c.3993C>A (p.Asp1331Glu)	not specified [RCV004667003]	uncertain significance	9	136466399	136466399	Human		name
407476932	CV3476645	single nucleotide variant	NM_014866.2(SEC16A):c.5168T>C (p.Met1723Thr)	not specified [RCV004663596]	uncertain significance	9	136459780	136459780	Human		name
407492020	CV3476647	single nucleotide variant	NM_014866.2(SEC16A):c.3323C>T (p.Ala1108Val)	not specified [RCV004667004]	uncertain significance	9	136474293	136474293	Human		name
407492027	CV3476649	single nucleotide variant	NM_014866.2(SEC16A):c.4064G>A (p.Arg1355Gln)	not specified [RCV004667006]	likely benign	9	136466328	136466328	Human		name
407492031	CV3476650	single nucleotide variant	NM_014866.2(SEC16A):c.4828G>C (p.Ala1610Pro)	not specified [RCV004667007]	uncertain significance	9	136462952	136462952	Human		name
407476941	CV3476651	single nucleotide variant	NM_014866.2(SEC16A):c.4553A>G (p.Lys1518Arg)	not specified [RCV004663598]	uncertain significance	9	136463557	136463557	Human		name
407476944	CV3476653	single nucleotide variant	NM_014866.2(SEC16A):c.4637G>A (p.Arg1546Lys)	not specified [RCV004663599]	uncertain significance	9	136463473	136463473	Human		name
407476955	CV3476658	single nucleotide variant	NM_014866.2(SEC16A):c.3142G>T (p.Ala1048Ser)	not specified [RCV004663601]	uncertain significance	9	136474474	136474474	Human		name
407476966	CV3476660	single nucleotide variant	NM_014866.2(SEC16A):c.6268A>G (p.Arg2090Gly)	not specified [RCV004663603]	uncertain significance	9	136451300	136451300	Human		name
407476971	CV3476661	single nucleotide variant	NM_014866.2(SEC16A):c.3755A>C (p.Gln1252Pro)	not specified [RCV004663604]	uncertain significance	9	136468462	136468462	Human		name
407476977	CV3476663	single nucleotide variant	NM_014866.2(SEC16A):c.6453A>T (p.Lys2151Asn)	not specified [RCV004663605]	uncertain significance	9	136447675	136447675	Human		name
597715305	CV3605406	single nucleotide variant	NM_014866.2(SEC16A):c.4100G>A (p.Arg1367His)	not specified [RCV004861448]	uncertain significance	9	136466292	136466292	Human		name
597715315	CV3605407	single nucleotide variant	NM_014866.2(SEC16A):c.3999T>G (p.Asp1333Glu)	not specified [RCV004861449]	likely benign	9	136466393	136466393	Human		name
597715323	CV3605408	single nucleotide variant	NM_014866.2(SEC16A):c.5383G>A (p.Glu1795Lys)	not specified [RCV004861450]	uncertain significance	9	136459160	136459160	Human		name
597715332	CV3605410	single nucleotide variant	NM_014866.2(SEC16A):c.6685G>A (p.Val2229Met)	not specified [RCV004861451]	uncertain significance	9	136447239	136447239	Human		name
597715352	CV3605412	single nucleotide variant	NM_014866.2(SEC16A):c.3461A>G (p.Gln1154Arg)	not specified [RCV004861453]	uncertain significance	9	136474155	136474155	Human		name
597715362	CV3605413	single nucleotide variant	NM_014866.2(SEC16A):c.3734C>A (p.Ser1245Tyr)	not specified [RCV004861454]	uncertain significance	9	136468483	136468483	Human		name
597715372	CV3605414	single nucleotide variant	NM_014866.2(SEC16A):c.5491A>C (p.Lys1831Gln)	not specified [RCV004861455]	uncertain significance	9	136457503	136457503	Human		name
597715383	CV3605415	single nucleotide variant	NM_014866.2(SEC16A):c.6458C>T (p.Pro2153Leu)	not specified [RCV004861456]	uncertain significance	9	136447670	136447670	Human		name
597715393	CV3605416	single nucleotide variant	NM_014866.2(SEC16A):c.6746C>T (p.Ala2249Val)	not specified [RCV004861457]	uncertain significance	9	136446901	136446901	Human		name
597715442	CV3605422	single nucleotide variant	NM_014866.2(SEC16A):c.4171G>A (p.Glu1391Lys)	not specified [RCV004861462]	uncertain significance	9	136466094	136466094	Human		name
597715453	CV3605423	single nucleotide variant	NM_014866.2(SEC16A):c.3088T>G (p.Ser1030Ala)	not specified [RCV004861463]	uncertain significance	9	136474528	136474528	Human		name
597715462	CV3605424	single nucleotide variant	NM_014866.2(SEC16A):c.3734C>G (p.Ser1245Cys)	not specified [RCV004861464]	uncertain significance	9	136468483	136468483	Human		name
597715472	CV3605425	single nucleotide variant	NM_014866.2(SEC16A):c.4685G>A (p.Arg1562Gln)	not specified [RCV004861465]	uncertain significance	9	136463095	136463095	Human		name
597715504	CV3605429	single nucleotide variant	NM_014866.2(SEC16A):c.6304C>T (p.Pro2102Ser)	not specified [RCV004861468]	uncertain significance	9	136451264	136451264	Human		name
597715513	CV3605430	single nucleotide variant	NM_014866.2(SEC16A):c.3946A>G (p.Asn1316Asp)	not specified [RCV004861469]	likely benign	9	136466446	136466446	Human		name
597715523	CV3605431	single nucleotide variant	NM_014866.2(SEC16A):c.4100G>C (p.Arg1367Pro)	not specified [RCV004861470]	uncertain significance	9	136466292	136466292	Human		name
597715534	CV3605432	single nucleotide variant	NM_014866.2(SEC16A):c.4282G>A (p.Val1428Ile)	not specified [RCV004861471]	uncertain significance	9	136465983	136465983	Human		name
597715555	CV3605434	single nucleotide variant	NM_014866.2(SEC16A):c.6535G>A (p.Val2179Met)	not specified [RCV004861473]	uncertain significance	9	136447593	136447593	Human		name
597715564	CV3605435	single nucleotide variant	NM_014866.2(SEC16A):c.6017G>A (p.Gly2006Asp)	not specified [RCV004861474]	uncertain significance	9	136454168	136454168	Human		name
597715606	CV3605440	single nucleotide variant	NM_014866.2(SEC16A):c.5774C>G (p.Ala1925Gly)	not specified [RCV004861478]	likely benign	9	136455684	136455684	Human		name
597715631	CV3605442	single nucleotide variant	NM_014866.2(SEC16A):c.5297A>G (p.Asn1766Ser)	not specified [RCV004861480]	uncertain significance	9	136459450	136459450	Human		name
597715652	CV3605444	single nucleotide variant	NM_014866.2(SEC16A):c.3644A>G (p.Tyr1215Cys)	not specified [RCV004861482]	uncertain significance	9	136472035	136472035	Human		name
597715683	CV3605447	single nucleotide variant	NM_014866.2(SEC16A):c.3512C>T (p.Pro1171Leu)	not specified [RCV004861485]	uncertain significance	9	136474104	136474104	Human		name
597715694	CV3605448	single nucleotide variant	NM_014866.2(SEC16A):c.4357A>G (p.Arg1453Gly)	not specified [RCV004861486]	uncertain significance	9	136464509	136464509	Human		name
597715706	CV3605449	single nucleotide variant	NM_014866.2(SEC16A):c.4372G>A (p.Gly1458Ser)	not specified [RCV004861487]	uncertain significance	9	136464494	136464494	Human		name
597715716	CV3605450	single nucleotide variant	NM_014866.2(SEC16A):c.4051G>C (p.Glu1351Gln)	not specified [RCV004861488]	uncertain significance	9	136466341	136466341	Human		name
598210407	CV3907113	single nucleotide variant	NM_014866.2(SEC16A):c.3954G>C (p.Trp1318Cys)	not specified [RCV005270664]	uncertain significance	9	136466438	136466438	Human		name
598210414	CV3907114	single nucleotide variant	NM_014866.2(SEC16A):c.3344G>C (p.Arg1115Pro)	not specified [RCV005270665]	uncertain significance	9	136474272	136474272	Human		name
598210420	CV3907115	single nucleotide variant	NM_014866.2(SEC16A):c.5642A>G (p.Gln1881Arg)	not specified [RCV005270666]	uncertain significance	9	136456075	136456075	Human		name
598210425	CV3907116	single nucleotide variant	NM_014866.2(SEC16A):c.4855G>A (p.Glu1619Lys)	not specified [RCV005270667]	uncertain significance	9	136462925	136462925	Human		name
598210436	CV3907118	single nucleotide variant	NM_014866.2(SEC16A):c.6656C>T (p.Ala2219Val)	not specified [RCV005270669]	uncertain significance	9	136447268	136447268	Human		name
598210442	CV3907119	single nucleotide variant	NM_014866.2(SEC16A):c.4448C>T (p.Ala1483Val)	not specified [RCV005270670]	uncertain significance	9	136463739	136463739	Human		name
598210450	CV3907120	single nucleotide variant	NM_014866.2(SEC16A):c.5906C>T (p.Pro1969Leu)	not specified [RCV005270671]	uncertain significance	9	136454279	136454279	Human		name
598210478	CV3907124	single nucleotide variant	NM_014866.2(SEC16A):c.6757G>A (p.Gly2253Ser)	not specified [RCV005270675]	uncertain significance	9	136446890	136446890	Human		name
598210500	CV3907127	single nucleotide variant	NM_014866.2(SEC16A):c.3988G>A (p.Asp1330Asn)	not specified [RCV005270678]	uncertain significance	9	136466404	136466404	Human		name
598210507	CV3907128	single nucleotide variant	NM_014866.2(SEC16A):c.5726G>A (p.Ser1909Asn)	not specified [RCV005270679]	uncertain significance	9	136455732	136455732	Human		name
598210557	CV3907136	single nucleotide variant	NM_014866.2(SEC16A):c.4149C>G (p.His1383Gln)	not specified [RCV005270687]	uncertain significance	9	136466116	136466116	Human		name
598210564	CV3907137	single nucleotide variant	NM_014866.2(SEC16A):c.3697C>T (p.Pro1233Ser)	not specified [RCV005270688]	uncertain significance	9	136471982	136471982	Human		name
15172105	CV700893	single nucleotide variant	NM_014866.2(SEC16A):c.6173C>T (p.Thr2058Met)	not provided [RCV000949955]	benign	9	136451395	136451395	Human		name
15190686	CV700894	single nucleotide variant	NM_014866.2(SEC16A):c.4125C>A (p.His1375Gln)	not provided [RCV000954550]	benign	9	136466267	136466267	Human		name
15158689	CV711865	single nucleotide variant	NM_014866.2(SEC16A):c.5702C>T (p.Pro1901Leu)	not provided [RCV000969566]	benign	9	136455756	136455756	Human		name
15158702	CV711867	single nucleotide variant	NM_014866.2(SEC16A):c.3066T>A (p.Ser1022Arg)	not provided [RCV000969568]	benign	9	136474550	136474550	Human		name
15162340	CV737015	single nucleotide variant	NM_014866.2(SEC16A):c.6676A>G (p.Asn2226Asp)	not provided [RCV000903532]	benign	9	136447248	136447248	Human		name
15163436	CV737016	single nucleotide variant	NM_014866.2(SEC16A):c.3934G>A (p.Glu1312Lys)	not provided [RCV000903773]	benign	9	136466458	136466458	Human		name
15122885	CV751562	single nucleotide variant	NM_014866.2(SEC16A):c.5867C>T (p.Thr1956Met)	not provided [RCV000918726]	likely benign	9	136454318	136454318	Human		name
401918683	CV2823612	microsatellite	NM_014866.2(SEC16A):c.1096TCAGGAGCT[1] (p.366SGA[1])	not provided [RCV003430405]	likely benign	9	136476503	136476511	Human		name

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